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Artigo de periodico
Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: a pilot study in Brazil (2024)
Migliavacca, Michele P ; Sobreira, Joselito ; Bermeo, Diana; Gomes, Mireille; Alencar, Dayse; Sussuchi, Luciane; Souza, Camila Alves; Silva, Juliana Santos; Kroll, José Eduardo; Burger, Matheus; Sousa, Rodrigo Guarischi ; Villela, Darine ; Yamamoto, Guilherme L ; Milanezi, Fernanda ; Horigoshi, Nelson; Cesar, Regina Grigolli; Carvalho, Werther Brunow de ; Honjo, Rachel Sayuri ; Bertola, Débora Romeo ; Kim, Chong Ae ; Souza, Lucian de; Procianoy, Renato S; Silveria, Rita C; Rosenberg, Carla ; Giugliani, Roberto ; Campana, Gustavo Aguiar; Scapulatempo-Neto, Cristovam ; Sobreira, Nara
Source: American Journal of Medical Genetics. Part A. Unidades: BIOINFORMÁTICA, FM, IB
Subjects: PEDIATRIA, SEQUENCIAMENTO GENÉTICO, DOENÇAS DO RECÉM-NASCIDO
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ABNT
MIGLIAVACCA, Michele P et al. Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: a pilot study in Brazil. American Journal of Medical Genetics. Part A, n. ja, 2024Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.63544. Acesso em: 29 maio 2024.
APA
Migliavacca, M. P., Sobreira, J., Bermeo, D., Gomes, M., Alencar, D., Sussuchi, L., et al. (2024). Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: a pilot study in Brazil. American Journal of Medical Genetics. Part A, (ja). doi:10.1002/ajmg.a.63544
NLM
Migliavacca MP, Sobreira J, Bermeo D, Gomes M, Alencar D, Sussuchi L, Souza CA, Silva JS, Kroll JE, Burger M, Sousa RG, Villela D, Yamamoto GL, Milanezi F, Horigoshi N, Cesar RG, Carvalho WB de, Honjo RS, Bertola DR, Kim CA, Souza L de, Procianoy RS, Silveria RC, Rosenberg C, Giugliani R, Campana GA, Scapulatempo-Neto C, Sobreira N. Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: a pilot study in Brazil [Internet]. American Journal of Medical Genetics. Part A. 2024 ;(ja):[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.63544
Vancouver
Migliavacca MP, Sobreira J, Bermeo D, Gomes M, Alencar D, Sussuchi L, Souza CA, Silva JS, Kroll JE, Burger M, Sousa RG, Villela D, Yamamoto GL, Milanezi F, Horigoshi N, Cesar RG, Carvalho WB de, Honjo RS, Bertola DR, Kim CA, Souza L de, Procianoy RS, Silveria RC, Rosenberg C, Giugliani R, Campana GA, Scapulatempo-Neto C, Sobreira N. Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: a pilot study in Brazil [Internet]. American Journal of Medical Genetics. Part A. 2024 ;(ja):[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.63544
Artigo de periodico
SCAF4-related syndromic intellectual disability (2023)
Carvalho, Laura Machado Lara ; Pinto, Carla Franchi; Scliar, Marília de Oliveira; Otto, Paulo A ; Krepischi, Ana Cristina Victorino ; Rosenberg, Carla
Source: American Journal of Medical Genetics. Part A. Unidade: IB
Subjects: GENÉTICA, PESSOAS COM DEFICIÊNCIA INTELECTUAL, GENES
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ABNT
CARVALHO, Laura Machado Lara et al. SCAF4-related syndromic intellectual disability. American Journal of Medical Genetics. Part A, v. 191, n. 2, p. 570-574, 2023Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.63032. Acesso em: 29 maio 2024.
APA
Carvalho, L. M. L., Pinto, C. F., Scliar, M. de O., Otto, P. A., Krepischi, A. C. V., & Rosenberg, C. (2023). SCAF4-related syndromic intellectual disability. American Journal of Medical Genetics. Part A, 191( 2), 570-574. doi:10.1002/ajmg.a.63032
NLM
Carvalho LML, Pinto CF, Scliar M de O, Otto PA, Krepischi ACV, Rosenberg C. SCAF4-related syndromic intellectual disability [Internet]. American Journal of Medical Genetics. Part A. 2023 ; 191( 2): 570-574.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.63032
Vancouver
Carvalho LML, Pinto CF, Scliar M de O, Otto PA, Krepischi ACV, Rosenberg C. SCAF4-related syndromic intellectual disability [Internet]. American Journal of Medical Genetics. Part A. 2023 ; 191( 2): 570-574.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.63032
Artigo de periodico
Updated consensus guidelines on the management of Phelan–McDermid syndrome (2023)
Srivastava, Siddharth ; Sahin, Mustafa ; Buxbaum, Joseph D ; Berry-Kravis, Elizabeth; Soorya, Latha Valluripalli; Thurm, Audrey ; Bernstein, Jonathan A ; Asante-Otoo, Afua; Bennett Jr, William E; Betancur, Catalina ; Brickhouse, Tegwyn H; Passos-Bueno, Maria Rita
Source: American Journal of Medical Genetics. Part A. Unidade: IB
Subjects: GENÉTICA MÉDICA, NEUROGENÉTICA
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ABNT
SRIVASTAVA, Siddharth et al. Updated consensus guidelines on the management of Phelan–McDermid syndrome. American Journal of Medical Genetics. Part A, v. 191, n. 8, p. 2015-2044, 2023Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.63312. Acesso em: 29 maio 2024.
APA
Srivastava, S., Sahin, M., Buxbaum, J. D., Berry-Kravis, E., Soorya, L. V., Thurm, A., et al. (2023). Updated consensus guidelines on the management of Phelan–McDermid syndrome. American Journal of Medical Genetics. Part A, 191( 8), 2015-2044. doi:10.1002/ajmg.a.63312
NLM
Srivastava S, Sahin M, Buxbaum JD, Berry-Kravis E, Soorya LV, Thurm A, Bernstein JA, Asante-Otoo A, Bennett Jr WE, Betancur C, Brickhouse TH, Passos-Bueno MR. Updated consensus guidelines on the management of Phelan–McDermid syndrome [Internet]. American Journal of Medical Genetics. Part A. 2023 ;191( 8): 2015-2044.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.63312
Vancouver
Srivastava S, Sahin M, Buxbaum JD, Berry-Kravis E, Soorya LV, Thurm A, Bernstein JA, Asante-Otoo A, Bennett Jr WE, Betancur C, Brickhouse TH, Passos-Bueno MR. Updated consensus guidelines on the management of Phelan–McDermid syndrome [Internet]. American Journal of Medical Genetics. Part A. 2023 ;191( 8): 2015-2044.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.63312
Artigo de periodico-carta/editorial
FMR1 premutation in children with autism spectrum disorders: should additional diagnostic tests be performed? (2022)
Girardi, Ana Cristina De Sanctis ; Takahashi, Vanessa Naomi Van Opstal ; Vadasz, Estêvão ; Costa, Claudia Ismania Samogi ; Zachi, Elaine Cristina; Vianna-Morgante, Angela M ; Passos-Bueno, Maria Rita
Source: American Journal of Medical Genetics. Part A. Unidades: IB, IP
Subjects: TRANSTORNO AUTÍSTICO, CRIANÇAS AUTISTAS
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ABNT
GIRARDI, Ana Cristina De Sanctis et al. FMR1 premutation in children with autism spectrum disorders: should additional diagnostic tests be performed?. American Journal of Medical Genetics. Part A. Hoboken, NJ: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1002/ajmg.a.62624. Acesso em: 29 maio 2024. , 2022
APA
Girardi, A. C. D. S., Takahashi, V. N. V. O., Vadasz, E., Costa, C. I. S., Zachi, E. C., Vianna-Morgante, A. M., & Passos-Bueno, M. R. (2022). FMR1 premutation in children with autism spectrum disorders: should additional diagnostic tests be performed? American Journal of Medical Genetics. Part A. Hoboken, NJ: Instituto de Biociências, Universidade de São Paulo. doi:10.1002/ajmg.a.62624
NLM
Girardi ACDS, Takahashi VNVO, Vadasz E, Costa CIS, Zachi EC, Vianna-Morgante AM, Passos-Bueno MR. FMR1 premutation in children with autism spectrum disorders: should additional diagnostic tests be performed? [Internet]. American Journal of Medical Genetics. Part A. 2022 ;188( 4): 1334-1337.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.62624
Vancouver
Girardi ACDS, Takahashi VNVO, Vadasz E, Costa CIS, Zachi EC, Vianna-Morgante AM, Passos-Bueno MR. FMR1 premutation in children with autism spectrum disorders: should additional diagnostic tests be performed? [Internet]. American Journal of Medical Genetics. Part A. 2022 ;188( 4): 1334-1337.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.62624
Artigo de periodico
Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses (2021)
Villela, Darine ; Mazzonetto, Patricia C; Migliavacca, Michele P; Perrone, Eduardo; Guida, Gustavo; Milanezi, Maria Fernanda G; Jorge, Alexander A. L ; Ribeiro-Bicudo, Lucilene A ; Kok, Fernando ; Campagnari, Francine; Rosso-Giuliani, Liane de; Costa, Silvia Souza da; Vianna-Morgante, Angela M ; Pearson, Peter L; Krepischi, Ana Cristina Victorino ; Rosenberg, Carla
Source: American Journal of Medical Genetics. Part A. Unidades: FM, IB
Subjects: DOENÇAS GENÉTICAS, DOENÇAS CONGÊNITAS, ANORMALIDADES CROMOSSÔMICAS, TRANSTORNO AUTÍSTICO
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ABNT
VILLELA, Darine et al. Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses. American Journal of Medical Genetics. Part A, v. 185, n. 8, p. 2335-2344, 2021Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.62237. Acesso em: 29 maio 2024.
APA
Villela, D., Mazzonetto, P. C., Migliavacca, M. P., Perrone, E., Guida, G., Milanezi, M. F. G., et al. (2021). Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses. American Journal of Medical Genetics. Part A, 185( 8), 2335-2344. doi:10.1002/ajmg.a.62237
NLM
Villela D, Mazzonetto PC, Migliavacca MP, Perrone E, Guida G, Milanezi MFG, Jorge AAL, Ribeiro-Bicudo LA, Kok F, Campagnari F, Rosso-Giuliani L de, Costa SS da, Vianna-Morgante AM, Pearson PL, Krepischi ACV, Rosenberg C. Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses [Internet]. American Journal of Medical Genetics. Part A. 2021 ; 185( 8): 2335-2344.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.62237
Vancouver
Villela D, Mazzonetto PC, Migliavacca MP, Perrone E, Guida G, Milanezi MFG, Jorge AAL, Ribeiro-Bicudo LA, Kok F, Campagnari F, Rosso-Giuliani L de, Costa SS da, Vianna-Morgante AM, Pearson PL, Krepischi ACV, Rosenberg C. Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses [Internet]. American Journal of Medical Genetics. Part A. 2021 ; 185( 8): 2335-2344.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.62237
Artigo de periodico
Down Syndrome in diverse populations (2017)
Kruszka, Paul; Porras, Antonio R.; Sobering, Andrew K.; Ikolo, Felicia A.; Qua, Samantha La; Shotelersuk, Vorasuk; Chung, Brian H. Y.; Mok, Gary T. K.; Uwineza, Annette; Mutesa, Leon; Moresco, Angélica; Obregon, María Gabriela; Sokunbi, Ogochukwu Jidechukwu; Kalu, Nnenna; Joseph, Daniel Akinsanya; Ikebudu, Desmond; Ugwu, Christopher Emeka; Okoromah, Christy A. N.; Addissie, Yonit A.; Pardo, Katherine L.; Brough, J. Joseph; Lee, Ni-Chung; Girisha, Katta M.; Patil, Siddaramappa Jagdish; Ng, Ivy S. L.; Min, Breana Cham Wen; Jamuar, Saumya S.; Tibrewal, Shailja; Wallang, Batriti; Ganesh, Suma; Sirisena, Nirmala D.; Dissanayake, Vajira H. W.; Paththinige, C. Sampath; Prabodha, L. B. Lahiru; Richieri-Costa, Antonio; Muthukumarasamy, Premala; Thong, Meow-Keong; Jones, Kelly L.; Abdul-Rahman, Omar A.; Ekure, Ekanem Nsikak; Adeyemo, Adebowale A.; Summar, Marshall; Linguraru, Marius George; Muenke, Maximilian
Source: American Journal of Medical Genetics. Part A. Unidade: HRAC
Assunto: SÍNDROME DE DOWN
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ABNT
KRUSZKA, Paul et al. Down Syndrome in diverse populations. American Journal of Medical Genetics. Part A, v. 173, n. Ja/2017, p. 42-53, 2017Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.38043. Acesso em: 29 maio 2024.
APA
Kruszka, P., Porras, A. R., Sobering, A. K., Ikolo, F. A., Qua, S. L., Shotelersuk, V., et al. (2017). Down Syndrome in diverse populations. American Journal of Medical Genetics. Part A, 173( Ja/2017), 42-53. doi:10.1002/ajmg.a.38043
NLM
Kruszka P, Porras AR, Sobering AK, Ikolo FA, Qua SL, Shotelersuk V, Chung BHY, Mok GTK, Uwineza A, Mutesa L, Moresco A, Obregon MG, Sokunbi OJ, Kalu N, Joseph DA, Ikebudu D, Ugwu CE, Okoromah CAN, Addissie YA, Pardo KL, Brough JJ, Lee N-C, Girisha KM, Patil SJ, Ng ISL, Min BCW, Jamuar SS, Tibrewal S, Wallang B, Ganesh S, Sirisena ND, Dissanayake VHW, Paththinige CS, Prabodha LBL, Richieri-Costa A, Muthukumarasamy P, Thong M-K, Jones KL, Abdul-Rahman OA, Ekure EN, Adeyemo AA, Summar M, Linguraru MG, Muenke M. Down Syndrome in diverse populations [Internet]. American Journal of Medical Genetics. Part A. 2017 ; 173( Ja/2017): 42-53.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.38043
Vancouver
Kruszka P, Porras AR, Sobering AK, Ikolo FA, Qua SL, Shotelersuk V, Chung BHY, Mok GTK, Uwineza A, Mutesa L, Moresco A, Obregon MG, Sokunbi OJ, Kalu N, Joseph DA, Ikebudu D, Ugwu CE, Okoromah CAN, Addissie YA, Pardo KL, Brough JJ, Lee N-C, Girisha KM, Patil SJ, Ng ISL, Min BCW, Jamuar SS, Tibrewal S, Wallang B, Ganesh S, Sirisena ND, Dissanayake VHW, Paththinige CS, Prabodha LBL, Richieri-Costa A, Muthukumarasamy P, Thong M-K, Jones KL, Abdul-Rahman OA, Ekure EN, Adeyemo AA, Summar M, Linguraru MG, Muenke M. Down Syndrome in diverse populations [Internet]. American Journal of Medical Genetics. Part A. 2017 ; 173( Ja/2017): 42-53.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.38043
Artigo de periodico
Apert and Crouzon syndromes: cognitive development, brain abnormalities, and molecular aspects (2016)
Fernandes, Marilyse B. L.; Maximino, Luciana P.; Perosa, Gimol B.; Abramides, Dagma V. M.; Passos-Bueno, Maria Rita ; Yacubian-Fernandes, Adriano
Source: American Journal of Medical Genetics. Part A. Unidades: FOB, IB
Subjects: CRANIOSSINOSTOSE, APTIDÃO COGNITIVA, SISTEMA NERVOSO CENTRAL, BIOLOGIA MOLECULAR, DISOSTOSE CRÂNIOFACIAL
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ABNT
FERNANDES, Marilyse B. L. et al. Apert and Crouzon syndromes: cognitive development, brain abnormalities, and molecular aspects. American Journal of Medical Genetics. Part A, v. 176, n. 6, p. 1532-1537, 2016Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.37640. Acesso em: 29 maio 2024.
APA
Fernandes, M. B. L., Maximino, L. P., Perosa, G. B., Abramides, D. V. M., Passos-Bueno, M. R., & Yacubian-Fernandes, A. (2016). Apert and Crouzon syndromes: cognitive development, brain abnormalities, and molecular aspects. American Journal of Medical Genetics. Part A, 176( 6), 1532-1537. doi:10.1002/ajmg.a.37640
NLM
Fernandes MBL, Maximino LP, Perosa GB, Abramides DVM, Passos-Bueno MR, Yacubian-Fernandes A. Apert and Crouzon syndromes: cognitive development, brain abnormalities, and molecular aspects [Internet]. American Journal of Medical Genetics. Part A. 2016 ; 176( 6): 1532-1537.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.37640
Vancouver
Fernandes MBL, Maximino LP, Perosa GB, Abramides DVM, Passos-Bueno MR, Yacubian-Fernandes A. Apert and Crouzon syndromes: cognitive development, brain abnormalities, and molecular aspects [Internet]. American Journal of Medical Genetics. Part A. 2016 ; 176( 6): 1532-1537.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.37640
Artigo de periodico
A compound heterozygote SLC26A2 mutation resulting in Robin Sequence, mild limbs shortness, accelerated carpal ossification, and multiple epiphysial dysplasia in two Brazilian sisters: a new intermediate phenotype between diastrophic dysplasia and recessive multiple epiphyseal dysplasia (2013)
Zechi-Ceide, Roseli Maria ; Moura, Priscila Padilha; Raskin, Salmo; Richieri-Costa, Antonio ; Guion-Almeida, Maria Leine
Source: American Journal of Medical Genetics. Part A. Unidades: HRAC, HRACF
Subjects: SÍNDROME DE PIERRE ROBIN, MUTAÇÃO, ANORMALIDADES MÚLTIPLAS
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ABNT
ZECHI-CEIDE, Roseli Maria et al. A compound heterozygote SLC26A2 mutation resulting in Robin Sequence, mild limbs shortness, accelerated carpal ossification, and multiple epiphysial dysplasia in two Brazilian sisters: a new intermediate phenotype between diastrophic dysplasia and recessive multiple epiphyseal dysplasia. American Journal of Medical Genetics. Part A, v. 161, n. 8, p. 2088-2094, 2013Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.36057. Acesso em: 29 maio 2024.
APA
Zechi-Ceide, R. M., Moura, P. P., Raskin, S., Richieri-Costa, A., & Guion-Almeida, M. L. (2013). A compound heterozygote SLC26A2 mutation resulting in Robin Sequence, mild limbs shortness, accelerated carpal ossification, and multiple epiphysial dysplasia in two Brazilian sisters: a new intermediate phenotype between diastrophic dysplasia and recessive multiple epiphyseal dysplasia. American Journal of Medical Genetics. Part A, 161( 8), 2088-2094. doi:10.1002/ajmg.a.36057
NLM
Zechi-Ceide RM, Moura PP, Raskin S, Richieri-Costa A, Guion-Almeida ML. A compound heterozygote SLC26A2 mutation resulting in Robin Sequence, mild limbs shortness, accelerated carpal ossification, and multiple epiphysial dysplasia in two Brazilian sisters: a new intermediate phenotype between diastrophic dysplasia and recessive multiple epiphyseal dysplasia [Internet]. American Journal of Medical Genetics. Part A. 2013 ; 161( 8): 2088-2094.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.36057
Vancouver
Zechi-Ceide RM, Moura PP, Raskin S, Richieri-Costa A, Guion-Almeida ML. A compound heterozygote SLC26A2 mutation resulting in Robin Sequence, mild limbs shortness, accelerated carpal ossification, and multiple epiphysial dysplasia in two Brazilian sisters: a new intermediate phenotype between diastrophic dysplasia and recessive multiple epiphyseal dysplasia [Internet]. American Journal of Medical Genetics. Part A. 2013 ; 161( 8): 2088-2094.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.36057
Artigo de periodico
Obesity with associated developmental delay and/or learning disability in patients exhibiting additional features: Report of novel pathogenic copy number variants (2013)
D'Angelo, Carla Sustek; Kohl, Ilana; Varela, Monica Castro; Castro, Cláudia Irene Emílio de; Kim, Chong Ae; Bertola, Débora Romeo; Lourenço, Charles Marques; Perez, Ana Beatriz Alvarez; Koiffmann, Celia Priszkulnik
Source: American Journal of Medical Genetics. Part A. Unidade: IB
Subjects: OBESIDADE, ANORMALIDADES CROMOSSÔMICAS, DEFICIÊNCIA MENTAL, GENÉTICA MÉDICA
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ABNT
D'ANGELO, Carla Sustek et al. Obesity with associated developmental delay and/or learning disability in patients exhibiting additional features: Report of novel pathogenic copy number variants. American Journal of Medical Genetics. Part A, v. 161, n. 3, p. 479-486, 2013Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.35761. Acesso em: 29 maio 2024.
APA
D'Angelo, C. S., Kohl, I., Varela, M. C., Castro, C. I. E. de, Kim, C. A., Bertola, D. R., et al. (2013). Obesity with associated developmental delay and/or learning disability in patients exhibiting additional features: Report of novel pathogenic copy number variants. American Journal of Medical Genetics. Part A, 161( 3), 479-486. doi:10.1002/ajmg.a.35761
NLM
D'Angelo CS, Kohl I, Varela MC, Castro CIE de, Kim CA, Bertola DR, Lourenço CM, Perez ABA, Koiffmann CP. Obesity with associated developmental delay and/or learning disability in patients exhibiting additional features: Report of novel pathogenic copy number variants [Internet]. American Journal of Medical Genetics. Part A. 2013 ; 161( 3): 479-486.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.35761
Vancouver
D'Angelo CS, Kohl I, Varela MC, Castro CIE de, Kim CA, Bertola DR, Lourenço CM, Perez ABA, Koiffmann CP. Obesity with associated developmental delay and/or learning disability in patients exhibiting additional features: Report of novel pathogenic copy number variants [Internet]. American Journal of Medical Genetics. Part A. 2013 ; 161( 3): 479-486.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.35761
Artigo de periodico
Non-overlapping 22q11.2 microdeletions in patients with oculo-auriculo-vertebral spectrum (2013)
Santos, Pollyanna Almeida Costa dos; Oliveira, Silviene Fabiana de; Freitas, Erika L.; Safatle, Heloisa Pires Neto; Rosenberg, Carla ; Ferrari, Iris; Mazzeu, Juliana Forte
Source: American Journal of Medical Genetics. Part A. Unidades: IB, FMRP
Subjects: DISOSTOSE MANDIBULOFACIAL, DESENVOLVIMENTO CRANIOFACIAL, GENÉTICA
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ABNT
SANTOS, Pollyanna Almeida Costa dos et al. Non-overlapping 22q11.2 microdeletions in patients with oculo-auriculo-vertebral spectrum. American Journal of Medical Genetics. Part A, v. 164, n. 2, p. 551–553, 2013Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.36231. Acesso em: 29 maio 2024.
APA
Santos, P. A. C. dos, Oliveira, S. F. de, Freitas, E. L., Safatle, H. P. N., Rosenberg, C., Ferrari, I., & Mazzeu, J. F. (2013). Non-overlapping 22q11.2 microdeletions in patients with oculo-auriculo-vertebral spectrum. American Journal of Medical Genetics. Part A, 164( 2), 551–553. doi:10.1002/ajmg.a.36231
NLM
Santos PAC dos, Oliveira SF de, Freitas EL, Safatle HPN, Rosenberg C, Ferrari I, Mazzeu JF. Non-overlapping 22q11.2 microdeletions in patients with oculo-auriculo-vertebral spectrum [Internet]. American Journal of Medical Genetics. Part A. 2013 ; 164( 2): 551–553.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.36231
Vancouver
Santos PAC dos, Oliveira SF de, Freitas EL, Safatle HPN, Rosenberg C, Ferrari I, Mazzeu JF. Non-overlapping 22q11.2 microdeletions in patients with oculo-auriculo-vertebral spectrum [Internet]. American Journal of Medical Genetics. Part A. 2013 ; 164( 2): 551–553.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.36231
Artigo de periodico
Insertional translocation of 15q25-q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridia (2012)
Simioni, Milena; Vieira, Tarsis Paiva; Sgardioli, Ilária Cristina; Freitas, Érika Lopes; Rosenberg, Carla ; Maurer-Morelli, Cláudia Vianna; Lopes-Cendes, Iscia; Fett-Conte, Agnes Cristina; Lopes, Vera Lúcia Gil da Silva
Source: American Journal of Medical Genetics. Part A. Unidade: IB
Subjects: HIBRIDIZAÇÃO, GENÔMICA
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ABNT
SIMIONI, Milena et al. Insertional translocation of 15q25-q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridia. American Journal of Medical Genetics. Part A, v. 158, n. 11, p. 2905-2910, 2012Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.35603. Acesso em: 29 maio 2024.
APA
Simioni, M., Vieira, T. P., Sgardioli, I. C., Freitas, É. L., Rosenberg, C., Maurer-Morelli, C. V., et al. (2012). Insertional translocation of 15q25-q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridia. American Journal of Medical Genetics. Part A, 158( 11), 2905-2910. doi:10.1002/ajmg.a.35603
NLM
Simioni M, Vieira TP, Sgardioli IC, Freitas ÉL, Rosenberg C, Maurer-Morelli CV, Lopes-Cendes I, Fett-Conte AC, Lopes VLG da S. Insertional translocation of 15q25-q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridia [Internet]. American Journal of Medical Genetics. Part A. 2012 ; 158( 11): 2905-2910.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.35603
Vancouver
Simioni M, Vieira TP, Sgardioli IC, Freitas ÉL, Rosenberg C, Maurer-Morelli CV, Lopes-Cendes I, Fett-Conte AC, Lopes VLG da S. Insertional translocation of 15q25-q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridia [Internet]. American Journal of Medical Genetics. Part A. 2012 ; 158( 11): 2905-2910.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.35603
Artigo de periodico
Analysis of MLL2 gene in the first Brazilian family with Kabuki syndrome (2012)
Nakata, Nancy Mizue Kokitsu ; Petrin, Aline Lourenço; Heard, Jason Paul; Pittoli, Siulan Vendramini Paulovich ; Henkle, Laura E.; Santos, Daniela Vera Cruz dos; Murray, Jeffrey Clark; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Part A. Unidades: HRAC, HRACF
Subjects: GENÉTICA MÉDICA, ANORMALIDADES CROMOSSÔMICAS, HEREDITARIEDADE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NAKATA, Nancy Mizue Kokitsu et al. Analysis of MLL2 gene in the first Brazilian family with Kabuki syndrome. American Journal of Medical Genetics. Part A, v. 158A, n. 8, p. 2003-2008, 2012Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.35454. Acesso em: 29 maio 2024.
APA
Nakata, N. M. K., Petrin, A. L., Heard, J. P., Pittoli, S. V. P., Henkle, L. E., Santos, D. V. C. dos, et al. (2012). Analysis of MLL2 gene in the first Brazilian family with Kabuki syndrome. American Journal of Medical Genetics. Part A, 158A( 8), 2003-2008. doi:10.1002/ajmg.a.35454
NLM
Nakata NMK, Petrin AL, Heard JP, Pittoli SVP, Henkle LE, Santos DVC dos, Murray JC, Richieri-Costa A. Analysis of MLL2 gene in the first Brazilian family with Kabuki syndrome [Internet]. American Journal of Medical Genetics. Part A. 2012 ; 158A( 8): 2003-2008.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.35454
Vancouver
Nakata NMK, Petrin AL, Heard JP, Pittoli SVP, Henkle LE, Santos DVC dos, Murray JC, Richieri-Costa A. Analysis of MLL2 gene in the first Brazilian family with Kabuki syndrome [Internet]. American Journal of Medical Genetics. Part A. 2012 ; 158A( 8): 2003-2008.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.35454
Artigo de periodico
Novel mutations in IRF6 in nonsyndromic cleft lip with or without cleft palate: when should IRF6 mutational screening be done? (2009)
Jehee, Fernanda Sarquis; Burin, Beatriz A.; Rocha, Kátia Maria da; Zechi-Ceide, Roseli Maria; Bueno, Daniela F.; Brito, Luciano; Souza, Josiane; Leal, Gabriela Ferraz; Richieri-Costa, Antonio; Alonso, Nivaldo; Otto, Paulo A ; Passos-Bueno, Maria Rita
Source: American Journal of Medical Genetics. Part A. Unidades: HRAC, IB
Subjects: MALFORMAÇÕES, LÁBIO FISSURADO, PALATO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
JEHEE, Fernanda Sarquis et al. Novel mutations in IRF6 in nonsyndromic cleft lip with or without cleft palate: when should IRF6 mutational screening be done?. American Journal of Medical Genetics. Part A, v. 149A, n. 6, p. 1319-1322, 2009Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.32849. Acesso em: 29 maio 2024.
APA
Jehee, F. S., Burin, B. A., Rocha, K. M. da, Zechi-Ceide, R. M., Bueno, D. F., Brito, L., et al. (2009). Novel mutations in IRF6 in nonsyndromic cleft lip with or without cleft palate: when should IRF6 mutational screening be done? American Journal of Medical Genetics. Part A, 149A( 6), 1319-1322. doi:10.1002/ajmg.a.32849
NLM
Jehee FS, Burin BA, Rocha KM da, Zechi-Ceide RM, Bueno DF, Brito L, Souza J, Leal GF, Richieri-Costa A, Alonso N, Otto PA, Passos-Bueno MR. Novel mutations in IRF6 in nonsyndromic cleft lip with or without cleft palate: when should IRF6 mutational screening be done? [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 149A( 6): 1319-1322.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.32849
Vancouver
Jehee FS, Burin BA, Rocha KM da, Zechi-Ceide RM, Bueno DF, Brito L, Souza J, Leal GF, Richieri-Costa A, Alonso N, Otto PA, Passos-Bueno MR. Novel mutations in IRF6 in nonsyndromic cleft lip with or without cleft palate: when should IRF6 mutational screening be done? [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 149A( 6): 1319-1322.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.32849
Artigo de periodico
Frontonasal dysplasia, severe neuropsychological delay, and midline central nervous system anomalies: report of 10 Brazilian male patients (2009)
Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Part A. Unidade: HRAC
Subjects: ANORMALIDADES CRANIOFACIAIS, RETARDO MENTAL, AGENESIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio. Frontonasal dysplasia, severe neuropsychological delay, and midline central nervous system anomalies: report of 10 Brazilian male patients. American Journal of Medical Genetics. Part A, v. 149A, n. 5, p. 1006-1011, 2009Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.32717. Acesso em: 29 maio 2024.
APA
Guion-Almeida, M. L., & Richieri-Costa, A. (2009). Frontonasal dysplasia, severe neuropsychological delay, and midline central nervous system anomalies: report of 10 Brazilian male patients. American Journal of Medical Genetics. Part A, 149A( 5), 1006-1011. doi:10.1002/ajmg.a.32717
NLM
Guion-Almeida ML, Richieri-Costa A. Frontonasal dysplasia, severe neuropsychological delay, and midline central nervous system anomalies: report of 10 Brazilian male patients [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 149A( 5): 1006-1011.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.32717
Vancouver
Guion-Almeida ML, Richieri-Costa A. Frontonasal dysplasia, severe neuropsychological delay, and midline central nervous system anomalies: report of 10 Brazilian male patients [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 149A( 5): 1006-1011.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.32717
Artigo de periodico
A rare case of trisomy 15 pter-q21.2 due to a de novo marker chromosome (2009)
Pancaro, Ade Nubia Xavier; Christofolini, Denise Maria; Kulikowski, Leslie Domenici; Belagero, Sintia Iole Nogueira; Belluco, Fernanda Teixeira da Silva; Varela, Monica Castro; Koiffmann, Celia Priszkulnik ; Yoshimoto, Maisa; Squire, Jeremy A.; Schiavon, Adriana V.; Heck, Benjamin; Melaragno, Maria Isabel
Source: American Journal of Medical Genetics. Part A. Unidade: IB
Assunto: CROMOSSOMO X
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PANCARO, Ade Nubia Xavier et al. A rare case of trisomy 15 pter-q21.2 due to a de novo marker chromosome. American Journal of Medical Genetics. Part A, v. 152A, p. 753-758, 2009Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.33308. Acesso em: 29 maio 2024.
APA
Pancaro, A. N. X., Christofolini, D. M., Kulikowski, L. D., Belagero, S. I. N., Belluco, F. T. da S., Varela, M. C., et al. (2009). A rare case of trisomy 15 pter-q21.2 due to a de novo marker chromosome. American Journal of Medical Genetics. Part A, 152A, 753-758. doi:10.1002/ajmg.a.33308
NLM
Pancaro ANX, Christofolini DM, Kulikowski LD, Belagero SIN, Belluco FT da S, Varela MC, Koiffmann CP, Yoshimoto M, Squire JA, Schiavon AV, Heck B, Melaragno MI. A rare case of trisomy 15 pter-q21.2 due to a de novo marker chromosome [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 152A 753-758.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.33308
Vancouver
Pancaro ANX, Christofolini DM, Kulikowski LD, Belagero SIN, Belluco FT da S, Varela MC, Koiffmann CP, Yoshimoto M, Squire JA, Schiavon AV, Heck B, Melaragno MI. A rare case of trisomy 15 pter-q21.2 due to a de novo marker chromosome [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 152A 753-758.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.33308
Artigo de periodico
Mandibulofacial syndrome with growth amd mental retardation, microcephaly, ear anomalies with skin tags, and cleft palate in a mother and her son: autosomal dominant or X-linked syndrome? (2009)
Guion-Almeida, Maria Leine; Vendramini-Pittoli, Siulan; Passos-Bueno, Maria Rita ; Zechi-Ceide, Roseli Maria
Source: American Journal of Medical Genetics. Part A. Unidades: HRAC, IB
Assunto: ANOMALIA CRANIOFACIAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUION-ALMEIDA, Maria Leine et al. Mandibulofacial syndrome with growth amd mental retardation, microcephaly, ear anomalies with skin tags, and cleft palate in a mother and her son: autosomal dominant or X-linked syndrome?. American Journal of Medical Genetics. Part A, v. 149A, p. 2762-2764, 2009Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.32816. Acesso em: 29 maio 2024.
APA
Guion-Almeida, M. L., Vendramini-Pittoli, S., Passos-Bueno, M. R., & Zechi-Ceide, R. M. (2009). Mandibulofacial syndrome with growth amd mental retardation, microcephaly, ear anomalies with skin tags, and cleft palate in a mother and her son: autosomal dominant or X-linked syndrome? American Journal of Medical Genetics. Part A, 149A, 2762-2764. doi:10.1002/ajmg.a.32816
NLM
Guion-Almeida ML, Vendramini-Pittoli S, Passos-Bueno MR, Zechi-Ceide RM. Mandibulofacial syndrome with growth amd mental retardation, microcephaly, ear anomalies with skin tags, and cleft palate in a mother and her son: autosomal dominant or X-linked syndrome? [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 149A 2762-2764.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.32816
Vancouver
Guion-Almeida ML, Vendramini-Pittoli S, Passos-Bueno MR, Zechi-Ceide RM. Mandibulofacial syndrome with growth amd mental retardation, microcephaly, ear anomalies with skin tags, and cleft palate in a mother and her son: autosomal dominant or X-linked syndrome? [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 149A 2762-2764.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.32816
Artigo de periodico
Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes (2009)
Zechi-Ceide, Roseli Maria; Ribeiro, Lucilene Arilho; Raskin, Salmo; Bertolacini, Claudia Danielli Pereira; Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Part A. Unidade: HRAC
Subjects: HOLOPROSENCEFALIA, FISSURA LÁBIOPALATINA BILATERAL, GENES, ANORMALIDADES MÚLTIPLAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZECHI-CEIDE, Roseli Maria et al. Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes. American Journal of Medical Genetics. Part A, v. 149A, n. 6, p. 1277-1279, 2009Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.32844. Acesso em: 29 maio 2024.
APA
Zechi-Ceide, R. M., Ribeiro, L. A., Raskin, S., Bertolacini, C. D. P., Guion-Almeida, M. L., & Richieri-Costa, A. (2009). Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes. American Journal of Medical Genetics. Part A, 149A( 6), 1277-1279. doi:10.1002/ajmg.a.32844
NLM
Zechi-Ceide RM, Ribeiro LA, Raskin S, Bertolacini CDP, Guion-Almeida ML, Richieri-Costa A. Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 149A( 6): 1277-1279.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.32844
Vancouver
Zechi-Ceide RM, Ribeiro LA, Raskin S, Bertolacini CDP, Guion-Almeida ML, Richieri-Costa A. Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 149A( 6): 1277-1279.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.32844
Artigo de periodico
Extending the phenotype of monosomy 1p36 syndrome and mapping of a critical region for obesity and hyperphagia (2009)
D'Angelo, Carla S; Kohl, Ilana; Varela, Monica Castro; Castro, Claudia I. E. de; Kim, Chong A; Bertola, Débora R; Lourenço, Charles M; Koiffmann, Celia Priszkulnik
Source: American Journal of Medical Genetics. Part A. Unidade: IB
Subjects: MALFORMAÇÕES, DELEÇÃO DE GENES, ANORMALIDADES CROMOSSÔMICAS, OBESIDADE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
D'ANGELO, Carla S et al. Extending the phenotype of monosomy 1p36 syndrome and mapping of a critical region for obesity and hyperphagia. American Journal of Medical Genetics. Part A, v. 152A, n. 1, p. 102-110, 2009Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.33160. Acesso em: 29 maio 2024.
APA
D'Angelo, C. S., Kohl, I., Varela, M. C., Castro, C. I. E. de, Kim, C. A., Bertola, D. R., et al. (2009). Extending the phenotype of monosomy 1p36 syndrome and mapping of a critical region for obesity and hyperphagia. American Journal of Medical Genetics. Part A, 152A( 1), 102-110. doi:10.1002/ajmg.a.33160
NLM
D'Angelo CS, Kohl I, Varela MC, Castro CIE de, Kim CA, Bertola DR, Lourenço CM, Koiffmann CP. Extending the phenotype of monosomy 1p36 syndrome and mapping of a critical region for obesity and hyperphagia [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 152A( 1): 102-110.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.33160
Vancouver
D'Angelo CS, Kohl I, Varela MC, Castro CIE de, Kim CA, Bertola DR, Lourenço CM, Koiffmann CP. Extending the phenotype of monosomy 1p36 syndrome and mapping of a critical region for obesity and hyperphagia [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 152A( 1): 102-110.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.33160
Artigo de periodico
Mucopolysaccharidoses in Brazil: what happens from birth to biochemical diagnosis ? (2008)
Vieira, Taiane; Schwartz, Ida; Muñoz, Verónica; Pinto, Louise; Steiner, Carlos; Ribeiro, Márcia; Boy, Raquel; Ferraz, Victor Evangelista de Faria; Paula, Ana de; Kim, Chong; Acosta, Angelina; Giugliani, Roberto
Source: American Journal of Medical Genetics. Part A. Unidade: FMRP
Subjects: GLICOSAMINOGLICANAS, ERROS INATOS DO METABOLISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VIEIRA, Taiane et al. Mucopolysaccharidoses in Brazil: what happens from birth to biochemical diagnosis ?. American Journal of Medical Genetics. Part A, v. 146A, n. 13, p. 1741-1747, 2008Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.32320. Acesso em: 29 maio 2024.
APA
Vieira, T., Schwartz, I., Muñoz, V., Pinto, L., Steiner, C., Ribeiro, M., et al. (2008). Mucopolysaccharidoses in Brazil: what happens from birth to biochemical diagnosis ? American Journal of Medical Genetics. Part A, 146A( 13), 1741-1747. doi:10.1002/ajmg.a.32320
NLM
Vieira T, Schwartz I, Muñoz V, Pinto L, Steiner C, Ribeiro M, Boy R, Ferraz VE de F, Paula A de, Kim C, Acosta A, Giugliani R. Mucopolysaccharidoses in Brazil: what happens from birth to biochemical diagnosis ? [Internet]. American Journal of Medical Genetics. Part A. 2008 ; 146A( 13): 1741-1747.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.32320
Vancouver
Vieira T, Schwartz I, Muñoz V, Pinto L, Steiner C, Ribeiro M, Boy R, Ferraz VE de F, Paula A de, Kim C, Acosta A, Giugliani R. Mucopolysaccharidoses in Brazil: what happens from birth to biochemical diagnosis ? [Internet]. American Journal of Medical Genetics. Part A. 2008 ; 146A( 13): 1741-1747.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.32320
Artigo de periodico
Major gene and multifactorial inheritance of mandibular prognathism (2008)
Cruz, Ricardo Machado; Krieger, Henrique; Ferreira, Ricardo; Mah, James; Hartsfield Jr., James; Oliveira, Silviene
Source: American Journal of Medical Genetics. Part A. Unidade: ICB
Assunto: PARASITOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CRUZ, Ricardo Machado et al. Major gene and multifactorial inheritance of mandibular prognathism. American Journal of Medical Genetics. Part A, v. 146A, n. 1, p. 71-77, 2008Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.32062. Acesso em: 29 maio 2024.
APA
Cruz, R. M., Krieger, H., Ferreira, R., Mah, J., Hartsfield Jr., J., & Oliveira, S. (2008). Major gene and multifactorial inheritance of mandibular prognathism. American Journal of Medical Genetics. Part A, 146A( 1), 71-77. doi:10.1002/ajmg.a.32062
NLM
Cruz RM, Krieger H, Ferreira R, Mah J, Hartsfield Jr. J, Oliveira S. Major gene and multifactorial inheritance of mandibular prognathism [Internet]. American Journal of Medical Genetics. Part A. 2008 ; 146A( 1): 71-77.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.32062
Vancouver
Cruz RM, Krieger H, Ferreira R, Mah J, Hartsfield Jr. J, Oliveira S. Major gene and multifactorial inheritance of mandibular prognathism [Internet]. American Journal of Medical Genetics. Part A. 2008 ; 146A( 1): 71-77.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/ajmg.a.32062

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