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Artigo de periodico
Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome (2019)
Richieri-Costa, Antonio ; Zechi-Ceide, Roseli Maria ; Souza, Rosana Maria Candido ; Monteiro, Rejane Alves de Carvalho; Tonello, Cristiano; Freitas, Mariana L. de; Nakata, Nancy Mizue Kokitsu ; Pittoli, Siulan Vendramini Paulovich ; Mazzeu, Juliana F; Overes, Madelief; Ali-Amin, Roza; van Slegtenhorst, Marjon; Hoefsloot, Lies H; Jehee, Fernanda S
Fonte: American Journal of Medical Genetics. Unidade: HRAC
Assuntos: GENÉTICA, HOLOPROSENCEFALIA, FISSURA LÁBIOPALATINA, ANORMALIDADES CRANIOFACIAIS
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ABNT
RICHIERI-COSTA, Antonio et al. Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome. American Journal of Medical Genetics, v. No 2019, n. 11, p. 2170-2177, 2019Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.61305. Acesso em: 24 out. 2025.
APA
Richieri-Costa, A., Zechi-Ceide, R. M., Souza, R. M. C., Monteiro, R. A. de C., Tonello, C., Freitas, M. L. de, et al. (2019). Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome. American Journal of Medical Genetics, No 2019( 11), 2170-2177. doi:10.1002/ajmg.a.61305
NLM
Richieri-Costa A, Zechi-Ceide RM, Souza RMC, Monteiro RA de C, Tonello C, Freitas ML de, Nakata NMK, Pittoli SVP, Mazzeu JF, Overes M, Ali-Amin R, van Slegtenhorst M, Hoefsloot LH, Jehee FS. Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome [Internet]. American Journal of Medical Genetics. 2019 ; No 2019( 11): 2170-2177.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.61305
Vancouver
Richieri-Costa A, Zechi-Ceide RM, Souza RMC, Monteiro RA de C, Tonello C, Freitas ML de, Nakata NMK, Pittoli SVP, Mazzeu JF, Overes M, Ali-Amin R, van Slegtenhorst M, Hoefsloot LH, Jehee FS. Holoprosencephaly, orofacial cleft, and frontonaso-orbital encephaloceles: genetic evaluation of a possible new syndrome [Internet]. American Journal of Medical Genetics. 2019 ; No 2019( 11): 2170-2177.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.61305
Artigo de periodico
Low serum fatty acid levels in pregnancies with fetal gastroschisis: a prospective study (2018)
Centofanti, Sandra Frankfurt; Francisco, Rossana Pulcineli Vieira; Philippi, Sonia Tucunduva ; Castro, Inar Alves de ; Hoshida, Mara Sandra; Curi, Rui; Brizot, Maria de Lourdes
Fonte: American Journal of Medical Genetics. Unidades: FM, FCF
Assuntos: ÁCIDOS GRAXOS, LIPÍDEOS, GRAVIDEZ
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ABNT
CENTOFANTI, Sandra Frankfurt et al. Low serum fatty acid levels in pregnancies with fetal gastroschisis: a prospective study. American Journal of Medical Genetics, v. 176, n. 4, p. 915-924, 2018Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.38638. Acesso em: 24 out. 2025.
APA
Centofanti, S. F., Francisco, R. P. V., Philippi, S. T., Castro, I. A. de, Hoshida, M. S., Curi, R., & Brizot, M. de L. (2018). Low serum fatty acid levels in pregnancies with fetal gastroschisis: a prospective study. American Journal of Medical Genetics, 176( 4), 915-924. doi:10.1002/ajmg.a.38638
NLM
Centofanti SF, Francisco RPV, Philippi ST, Castro IA de, Hoshida MS, Curi R, Brizot M de L. Low serum fatty acid levels in pregnancies with fetal gastroschisis: a prospective study [Internet]. American Journal of Medical Genetics. 2018 ; 176( 4): 915-924.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.38638
Vancouver
Centofanti SF, Francisco RPV, Philippi ST, Castro IA de, Hoshida MS, Curi R, Brizot M de L. Low serum fatty acid levels in pregnancies with fetal gastroschisis: a prospective study [Internet]. American Journal of Medical Genetics. 2018 ; 176( 4): 915-924.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.38638
Artigo de periodico
Ablepharon macrostomia syndrome: a distinct genetic entity clinically related to the group of FRAS–FREM complex disorders (2013)
Schanze, Denny; Harakalova, Magdalena; Stevens, Cathy A.; Brancati, Francesco; Dallapiccola, Bruno; Farndon, Peter; Ferraz, Victor Evangelista de Faria; McGinn, Donna M. McDonald; Zackai, Elaine H.; Wright, Michael; Lieshout, Stef van; Vogel, Maartje J.; Haelst, Mieke M. van; Zenker, Martin
Fonte: American Journal of Medical Genetics. Unidade: FMRP
Assunto: MALFORMAÇÕES (GENÉTICA)
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ABNT
SCHANZE, Denny et al. Ablepharon macrostomia syndrome: a distinct genetic entity clinically related to the group of FRAS–FREM complex disorders. American Journal of Medical Genetics, v. 161A, n. 12, p. 3012\20133017, 2013Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.36119. Acesso em: 24 out. 2025.
APA
Schanze, D., Harakalova, M., Stevens, C. A., Brancati, F., Dallapiccola, B., Farndon, P., et al. (2013). Ablepharon macrostomia syndrome: a distinct genetic entity clinically related to the group of FRAS–FREM complex disorders. American Journal of Medical Genetics, 161A( 12), 3012\20133017. doi:10.1002/ajmg.a.36119
NLM
Schanze D, Harakalova M, Stevens CA, Brancati F, Dallapiccola B, Farndon P, Ferraz VE de F, McGinn DMMD, Zackai EH, Wright M, Lieshout S van, Vogel MJ, Haelst MM van, Zenker M. Ablepharon macrostomia syndrome: a distinct genetic entity clinically related to the group of FRAS–FREM complex disorders [Internet]. American Journal of Medical Genetics. 2013 ; 161A( 12): 3012\20133017.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.36119
Vancouver
Schanze D, Harakalova M, Stevens CA, Brancati F, Dallapiccola B, Farndon P, Ferraz VE de F, McGinn DMMD, Zackai EH, Wright M, Lieshout S van, Vogel MJ, Haelst MM van, Zenker M. Ablepharon macrostomia syndrome: a distinct genetic entity clinically related to the group of FRAS–FREM complex disorders [Internet]. American Journal of Medical Genetics. 2013 ; 161A( 12): 3012\20133017.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.36119
Artigo de periodico
Two new brazilian patients with Gómez-López-Hernández syndrome: reviewing the expanded phenotype with molecular insights (2008)
Gomy, Israel; Heck, Benjamin; Santos, Antonio Carlos dos; Figueiredo, Maria Silvia L.; Martinelli Júnior, Carlos Eduardo; Nogueira, Maria Priscila C.; Pina-Neto, João Monteiro
Fonte: American Journal of Medical Genetics. Unidade: FMRP
Assuntos: DOENÇAS DO SISTEMA NERVOSO CENTRAL, MANIFESTAÇÕES NEUROLÓGICAS
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ABNT
GOMY, Israel et al. Two new brazilian patients with Gómez-López-Hernández syndrome: reviewing the expanded phenotype with molecular insights. American Journal of Medical Genetics, v. 146A, p. 649-657, 2008Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.32173. Acesso em: 24 out. 2025.
APA
Gomy, I., Heck, B., Santos, A. C. dos, Figueiredo, M. S. L., Martinelli Júnior, C. E., Nogueira, M. P. C., & Pina-Neto, J. M. (2008). Two new brazilian patients with Gómez-López-Hernández syndrome: reviewing the expanded phenotype with molecular insights. American Journal of Medical Genetics, 146A, 649-657. doi:10.1002/ajmg.a.32173
NLM
Gomy I, Heck B, Santos AC dos, Figueiredo MSL, Martinelli Júnior CE, Nogueira MPC, Pina-Neto JM. Two new brazilian patients with Gómez-López-Hernández syndrome: reviewing the expanded phenotype with molecular insights [Internet]. American Journal of Medical Genetics. 2008 ; 146A 649-657.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.32173
Vancouver
Gomy I, Heck B, Santos AC dos, Figueiredo MSL, Martinelli Júnior CE, Nogueira MPC, Pina-Neto JM. Two new brazilian patients with Gómez-López-Hernández syndrome: reviewing the expanded phenotype with molecular insights [Internet]. American Journal of Medical Genetics. 2008 ; 146A 649-657.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.32173
Artigo de periodico
Preliminary molecular studies on blepharocheilodontic syndrome (2007)
Freitas, Érika L.; Martinhago, Ciro D.; Ramos, Ester Silveira; Murray, Jeffrey C.; Gil-da-Silva-Lopes, Vera L.
Fonte: American Journal of Medical Genetics. Unidade: FMRP
Assunto: ANORMALIDADES CRANIOFACIAIS
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ABNT
FREITAS, Érika L. et al. Preliminary molecular studies on blepharocheilodontic syndrome. American Journal of Medical Genetics, v. 143A, n. 22, p. 2757-2759, 2007Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.32010. Acesso em: 24 out. 2025.
APA
Freitas, É. L., Martinhago, C. D., Ramos, E. S., Murray, J. C., & Gil-da-Silva-Lopes, V. L. (2007). Preliminary molecular studies on blepharocheilodontic syndrome. American Journal of Medical Genetics, 143A( 22), 2757-2759. doi:10.1002/ajmg.a.32010
NLM
Freitas ÉL, Martinhago CD, Ramos ES, Murray JC, Gil-da-Silva-Lopes VL. Preliminary molecular studies on blepharocheilodontic syndrome [Internet]. American Journal of Medical Genetics. 2007 ; 143A( 22): 2757-2759.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.32010
Vancouver
Freitas ÉL, Martinhago CD, Ramos ES, Murray JC, Gil-da-Silva-Lopes VL. Preliminary molecular studies on blepharocheilodontic syndrome [Internet]. American Journal of Medical Genetics. 2007 ; 143A( 22): 2757-2759.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.32010
Artigo de periodico
An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome (2005)
Jehee, Fernanda Sarquis; Rosenberg, Carla ; Krepischi, Ana Cristina Victorino ; Kok, Fernando; Knijnenburg, Jeroen; Froyen, Guy; Vianna-Morgante, Angela M ; Opitz, John M.; Passos-Bueno, Maria Rita
Fonte: American Journal of Medical Genetics. Unidade: IB
Assuntos: CROMOSSOMO X (ANOMALIAS), MALFORMAÇÕES, DOENÇAS GENÉTICAS
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ABNT
JEHEE, Fernanda Sarquis et al. An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome. American Journal of Medical Genetics, v. 139A, n. 3, p. 221-225, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30991. Acesso em: 24 out. 2025.
APA
Jehee, F. S., Rosenberg, C., Krepischi, A. C. V., Kok, F., Knijnenburg, J., Froyen, G., et al. (2005). An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome. American Journal of Medical Genetics, 139A( 3), 221-225. doi:10.1002/ajmg.a.30991
NLM
Jehee FS, Rosenberg C, Krepischi ACV, Kok F, Knijnenburg J, Froyen G, Vianna-Morgante AM, Opitz JM, Passos-Bueno MR. An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome [Internet]. American Journal of Medical Genetics. 2005 ; 139A( 3): 221-225.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.30991
Vancouver
Jehee FS, Rosenberg C, Krepischi ACV, Kok F, Knijnenburg J, Froyen G, Vianna-Morgante AM, Opitz JM, Passos-Bueno MR. An Xq22.3 duplication detected by comparative genomic hybridization microarray (Array-CGH) defines a new locus (FGS5) for FG syndrome [Internet]. American Journal of Medical Genetics. 2005 ; 139A( 3): 221-225.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.30991
Artigo de periodico-carta/editorial
Newly recognized overgrowth syndrome with macrosomia, macrocrania, hyperostosis of the cranial vault, mental deficiency, seizures, poor motor control, and orofacial dyspraxia (2005)
Vitto, Luciana Paula Maximino de; Abramides, Dagma Venturini Marques; Richieri-Costa, Antonio
Fonte: American Journal of Medical Genetics. Unidade: FOB
Assuntos: GENÉTICA MÉDICA, RETARDO MENTAL, CONTROLE MOTOR
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ABNT
VITTO, Luciana Paula Maximino de e ABRAMIDES, Dagma Venturini Marques e RICHIERI-COSTA, Antonio. Newly recognized overgrowth syndrome with macrosomia, macrocrania, hyperostosis of the cranial vault, mental deficiency, seizures, poor motor control, and orofacial dyspraxia. American Journal of Medical Genetics. New York: Faculdade de Odontologia de Bauru, Universidade de São Paulo. Disponível em: http://www3.interscience.wiley.com/cgi-bin/fulltext/110522538/PDFSTART. Acesso em: 24 out. 2025. , 2005
APA
Vitto, L. P. M. de, Abramides, D. V. M., & Richieri-Costa, A. (2005). Newly recognized overgrowth syndrome with macrosomia, macrocrania, hyperostosis of the cranial vault, mental deficiency, seizures, poor motor control, and orofacial dyspraxia. American Journal of Medical Genetics. New York: Faculdade de Odontologia de Bauru, Universidade de São Paulo. Recuperado de http://www3.interscience.wiley.com/cgi-bin/fulltext/110522538/PDFSTART
NLM
Vitto LPM de, Abramides DVM, Richieri-Costa A. Newly recognized overgrowth syndrome with macrosomia, macrocrania, hyperostosis of the cranial vault, mental deficiency, seizures, poor motor control, and orofacial dyspraxia [Internet]. American Journal of Medical Genetics. 2005 ; 136A( 2): 219-220.[citado 2025 out. 24 ] Available from: http://www3.interscience.wiley.com/cgi-bin/fulltext/110522538/PDFSTART
Vancouver
Vitto LPM de, Abramides DVM, Richieri-Costa A. Newly recognized overgrowth syndrome with macrosomia, macrocrania, hyperostosis of the cranial vault, mental deficiency, seizures, poor motor control, and orofacial dyspraxia [Internet]. American Journal of Medical Genetics. 2005 ; 136A( 2): 219-220.[citado 2025 out. 24 ] Available from: http://www3.interscience.wiley.com/cgi-bin/fulltext/110522538/PDFSTART
Trabalho de evento-resumo periodico
Association between low amplitude P3 and DRD4 polymorphisms in 8-years old children (2005)
Vogel, C. I.; Laucht, M.; Furtado, Erikson Felipe; Schimidt, M. H.
Fonte: American Journal of Medical Genetics. Nome do evento: Annual Meeting of The American Society of Human Genetics. Unidade: FMRP
Assuntos: POLIMORFISMO, CRIANÇAS
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ABNT
VOGEL, C. I. et al. Association between low amplitude P3 and DRD4 polymorphisms in 8-years old children. American Journal of Medical Genetics. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 24 out. 2025. , 2005
APA
Vogel, C. I., Laucht, M., Furtado, E. F., & Schimidt, M. H. (2005). Association between low amplitude P3 and DRD4 polymorphisms in 8-years old children. American Journal of Medical Genetics. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Vogel CI, Laucht M, Furtado EF, Schimidt MH. Association between low amplitude P3 and DRD4 polymorphisms in 8-years old children. American Journal of Medical Genetics. 2005 ; 138B( 1): 53.[citado 2025 out. 24 ]
Vancouver
Vogel CI, Laucht M, Furtado EF, Schimidt MH. Association between low amplitude P3 and DRD4 polymorphisms in 8-years old children. American Journal of Medical Genetics. 2005 ; 138B( 1): 53.[citado 2025 out. 24 ]
Artigo de periodico
Polymorphisms in the methylenetetrahydrofolate reductase and methionine synthase reductase genes and homocysteine levels in brazilian children (2004)
Aléssio, Ana Claudia M.; Annichio-Bizzachi, Joyce M.; Bydlowski, Sérgio Paulo; Eberlin, Marcos N.; Vellasco, Adriana P.; Höehr, Nelci Fenalti
Fonte: American Journal of Medical Genetics. Unidade: FM
Assuntos: POLIMORFISMO, GENES, FATORES DE RISCO, DOENÇAS CARDIOVASCULARES (PREVENÇÃO E CONTROLE), CRIANÇAS
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ABNT
ALÉSSIO, Ana Claudia M. et al. Polymorphisms in the methylenetetrahydrofolate reductase and methionine synthase reductase genes and homocysteine levels in brazilian children. American Journal of Medical Genetics, v. 128A, n. 3, p. 256-260, 2004Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30108. Acesso em: 24 out. 2025.
APA
Aléssio, A. C. M., Annichio-Bizzachi, J. M., Bydlowski, S. P., Eberlin, M. N., Vellasco, A. P., & Höehr, N. F. (2004). Polymorphisms in the methylenetetrahydrofolate reductase and methionine synthase reductase genes and homocysteine levels in brazilian children. American Journal of Medical Genetics, 128A( 3), 256-260. doi:10.1002/ajmg.a.30108
NLM
Aléssio ACM, Annichio-Bizzachi JM, Bydlowski SP, Eberlin MN, Vellasco AP, Höehr NF. Polymorphisms in the methylenetetrahydrofolate reductase and methionine synthase reductase genes and homocysteine levels in brazilian children [Internet]. American Journal of Medical Genetics. 2004 ; 128A( 3): 256-260.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.30108
Vancouver
Aléssio ACM, Annichio-Bizzachi JM, Bydlowski SP, Eberlin MN, Vellasco AP, Höehr NF. Polymorphisms in the methylenetetrahydrofolate reductase and methionine synthase reductase genes and homocysteine levels in brazilian children [Internet]. American Journal of Medical Genetics. 2004 ; 128A( 3): 256-260.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.30108
Artigo de periodico
Unusual nasal duplication in two patients (2004)
Guion-Almeida, Maria Leine; Lamônica Neto, Domingos; Lopes, Vera Lúcia Gil da Silva
Fonte: American Journal of Medical Genetics. Unidade: HRAC
Assuntos: NARIZ (ANATOMIA), TOMOGRAFIA COMPUTADORIZADA POR RAIOS X, FENÓTIPOS
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ABNT
GUION-ALMEIDA, Maria Leine e LAMÔNICA NETO, Domingos e LOPES, Vera Lúcia Gil da Silva. Unusual nasal duplication in two patients. American Journal of Medical Genetics, v. No 2004, n. 4, p. 435-436, 2004Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30278. Acesso em: 24 out. 2025.
APA
Guion-Almeida, M. L., Lamônica Neto, D., & Lopes, V. L. G. da S. (2004). Unusual nasal duplication in two patients. American Journal of Medical Genetics, No 2004( 4), 435-436. doi:10.1002/ajmg.a.30278
NLM
Guion-Almeida ML, Lamônica Neto D, Lopes VLG da S. Unusual nasal duplication in two patients [Internet]. American Journal of Medical Genetics. 2004 ; No 2004( 4): 435-436.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.30278
Vancouver
Guion-Almeida ML, Lamônica Neto D, Lopes VLG da S. Unusual nasal duplication in two patients [Internet]. American Journal of Medical Genetics. 2004 ; No 2004( 4): 435-436.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.30278
Artigo de periodico
Five haplotypes account for fifty-five percent of ATM mutations in brazilian patients with ataxia telangiectasia: seven new mutations (2004)
Coutinho, Gabriela; Mitui, Midori; Campbell, Catarina; Carvalho, Beatriz T. Costa; Nahas, Shareef; Sun, Xia; Huo, Yong; Lai, Chih-hung; Thorstenson, Yvonne; Tanouye, Robert; Raskin, Salmo; Kim, Chong Ae; Llerena Junior, Juan; Gatti, Richard A.
Fonte: American Journal of Medical Genetics. Unidade: FM
Assuntos: DOENÇAS DO SISTEMA NERVOSO (GENÉTICA), DOENÇAS DO SISTEMA NERVOSO CENTRAL (GENÉTICA), GENÉTICA MOLECULAR, FAMÍLIA, POLIMORFISMO, BRASIL
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ABNT
COUTINHO, Gabriela et al. Five haplotypes account for fifty-five percent of ATM mutations in brazilian patients with ataxia telangiectasia: seven new mutations. American Journal of Medical Genetics, v. 126A, n. 1, p. 33-40, 2004Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.20570. Acesso em: 24 out. 2025.
APA
Coutinho, G., Mitui, M., Campbell, C., Carvalho, B. T. C., Nahas, S., Sun, X., et al. (2004). Five haplotypes account for fifty-five percent of ATM mutations in brazilian patients with ataxia telangiectasia: seven new mutations. American Journal of Medical Genetics, 126A( 1), 33-40. doi:10.1002/ajmg.a.20570
NLM
Coutinho G, Mitui M, Campbell C, Carvalho BTC, Nahas S, Sun X, Huo Y, Lai C-hung, Thorstenson Y, Tanouye R, Raskin S, Kim CA, Llerena Junior J, Gatti RA. Five haplotypes account for fifty-five percent of ATM mutations in brazilian patients with ataxia telangiectasia: seven new mutations [Internet]. American Journal of Medical Genetics. 2004 ; 126A( 1): 33-40.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.20570
Vancouver
Coutinho G, Mitui M, Campbell C, Carvalho BTC, Nahas S, Sun X, Huo Y, Lai C-hung, Thorstenson Y, Tanouye R, Raskin S, Kim CA, Llerena Junior J, Gatti RA. Five haplotypes account for fifty-five percent of ATM mutations in brazilian patients with ataxia telangiectasia: seven new mutations [Internet]. American Journal of Medical Genetics. 2004 ; 126A( 1): 33-40.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.20570
Artigo de periodico
Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? (2004)
Guion-Almeida, Maria Leine; Paula, Ligiane Alves Machado; Richieri-Costa, Antonio
Fonte: American Journal of Medical Genetics. Unidade: HRAC
Assunto: ANORMALIDADES MÚLTIPLAS
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ABNT
GUION-ALMEIDA, Maria Leine e PAULA, Ligiane Alves Machado e RICHIERI-COSTA, Antonio. Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome?. American Journal of Medical Genetics, v. 129A, n. 2, p. 156-161, 2004Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30153. Acesso em: 24 out. 2025.
APA
Guion-Almeida, M. L., Paula, L. A. M., & Richieri-Costa, A. (2004). Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? American Journal of Medical Genetics, 129A( 2), 156-161. doi:10.1002/ajmg.a.30153
NLM
Guion-Almeida ML, Paula LAM, Richieri-Costa A. Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? [Internet]. American Journal of Medical Genetics. 2004 ; 129A( 2): 156-161.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.30153
Vancouver
Guion-Almeida ML, Paula LAM, Richieri-Costa A. Newly recognized syndrome with heminasal aplasia and ocular anomalies or wider spectrum of heminasal aplasia/atypical clefting syndrome? [Internet]. American Journal of Medical Genetics. 2004 ; 129A( 2): 156-161.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.30153
Artigo de periodico-carta/editorial
TSPY detection in blood, buccal, and urine cells of patients with 45,X karyotype [Carta] (2004)
Bartmann, Ana Karina; Ramos, Ester Silveira; Caetano, Lisandra C.; Rios, Álvaro Fabrício Lopes; Vila, Reginaldo A.
Fonte: American Journal of Medical Genetics. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
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ABNT
BARTMANN, Ana Karina et al. TSPY detection in blood, buccal, and urine cells of patients with 45,X karyotype [Carta]. American Journal of Medical Genetics. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 24 out. 2025. , 2004
APA
Bartmann, A. K., Ramos, E. S., Caetano, L. C., Rios, Á. F. L., & Vila, R. A. (2004). TSPY detection in blood, buccal, and urine cells of patients with 45,X karyotype [Carta]. American Journal of Medical Genetics. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Bartmann AK, Ramos ES, Caetano LC, Rios ÁFL, Vila RA. TSPY detection in blood, buccal, and urine cells of patients with 45,X karyotype [Carta]. American Journal of Medical Genetics. 2004 ; 130A 320-321.[citado 2025 out. 24 ]
Vancouver
Bartmann AK, Ramos ES, Caetano LC, Rios ÁFL, Vila RA. TSPY detection in blood, buccal, and urine cells of patients with 45,X karyotype [Carta]. American Journal of Medical Genetics. 2004 ; 130A 320-321.[citado 2025 out. 24 ]
Artigo de periodico-carta/editorial
Blepharo-Cheilo-Dontic (BCD) syndrome with agenesis of thyroid broadens the phenotype and extends the discussion about the genes [Carta] (2004)
Martinhago, Ciro Dresch; Ramos, Ester Silveira
Fonte: American Journal of Medical Genetics. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARTINHAGO, Ciro Dresch e RAMOS, Ester Silveira. Blepharo-Cheilo-Dontic (BCD) syndrome with agenesis of thyroid broadens the phenotype and extends the discussion about the genes [Carta]. American Journal of Medical Genetics. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 24 out. 2025. , 2004
APA
Martinhago, C. D., & Ramos, E. S. (2004). Blepharo-Cheilo-Dontic (BCD) syndrome with agenesis of thyroid broadens the phenotype and extends the discussion about the genes [Carta]. American Journal of Medical Genetics. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Martinhago CD, Ramos ES. Blepharo-Cheilo-Dontic (BCD) syndrome with agenesis of thyroid broadens the phenotype and extends the discussion about the genes [Carta]. American Journal of Medical Genetics. 2004 ; 130A 437-438.[citado 2025 out. 24 ]
Vancouver
Martinhago CD, Ramos ES. Blepharo-Cheilo-Dontic (BCD) syndrome with agenesis of thyroid broadens the phenotype and extends the discussion about the genes [Carta]. American Journal of Medical Genetics. 2004 ; 130A 437-438.[citado 2025 out. 24 ]
Artigo de periodico
Expression of class 'mü' Glutathione-S-Transferase in human liver and its association with hepatopathies (2003)
Engracia, V.; Leite, M. M. B. S.; Pagotto, Rubiani de Cassia; Zucoloto, Sérgio; Barbosa, C. A. A.; Mestriner, Moacyr Antonio
Fonte: American Journal of Medical Genetics. Unidade: FMRP
Assuntos: HEPATOPATIAS, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ENGRACIA, V. et al. Expression of class 'mü' Glutathione-S-Transferase in human liver and its association with hepatopathies. American Journal of Medical Genetics, n. 123A, p. 257-260, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.20364. Acesso em: 24 out. 2025.
APA
Engracia, V., Leite, M. M. B. S., Pagotto, R. de C., Zucoloto, S., Barbosa, C. A. A., & Mestriner, M. A. (2003). Expression of class 'mü' Glutathione-S-Transferase in human liver and its association with hepatopathies. American Journal of Medical Genetics, ( 123A), 257-260. doi:10.1002/ajmg.a.20364
NLM
Engracia V, Leite MMBS, Pagotto R de C, Zucoloto S, Barbosa CAA, Mestriner MA. Expression of class 'mü' Glutathione-S-Transferase in human liver and its association with hepatopathies [Internet]. American Journal of Medical Genetics. 2003 ;( 123A): 257-260.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.20364
Vancouver
Engracia V, Leite MMBS, Pagotto R de C, Zucoloto S, Barbosa CAA, Mestriner MA. Expression of class 'mü' Glutathione-S-Transferase in human liver and its association with hepatopathies [Internet]. American Journal of Medical Genetics. 2003 ;( 123A): 257-260.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.20364
Artigo de periodico
Aural atresia and microtia in Kabuki syndrome [Research Letter] (2003)
Nakata, Nancy Mizue Kokitsu; Guion-Almeida, Maria Leine
Fonte: American Journal of Medical Genetics. Unidade: HRAC
Assunto: ANORMALIDADES MÚLTIPLAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NAKATA, Nancy Mizue Kokitsu e GUION-ALMEIDA, Maria Leine. Aural atresia and microtia in Kabuki syndrome [Research Letter]. American Journal of Medical Genetics, v. 118A, n. 4, p. 391-393, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.10189. Acesso em: 24 out. 2025.
APA
Nakata, N. M. K., & Guion-Almeida, M. L. (2003). Aural atresia and microtia in Kabuki syndrome [Research Letter]. American Journal of Medical Genetics, 118A( 4), 391-393. doi:10.1002/ajmg.a.10189
NLM
Nakata NMK, Guion-Almeida ML. Aural atresia and microtia in Kabuki syndrome [Research Letter] [Internet]. American Journal of Medical Genetics. 2003 ; 118A( 4): 391-393.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.10189
Vancouver
Nakata NMK, Guion-Almeida ML. Aural atresia and microtia in Kabuki syndrome [Research Letter] [Internet]. American Journal of Medical Genetics. 2003 ; 118A( 4): 391-393.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.10189
Trabalho de evento-resumo periodico
Candiddate genes for Tourette's: the DAT1 and 5HT1Dbeta preliminary results (2003)
Ramos Castillo, J. C.; Castillo, A.; Velloso, I.; Miguita, K.; Ekinaga, E.; Correa, R.; Biason, L.; Nunes, L.; Castro, A.; Gosling, F.; Halpern, B.; Miguel, Euripides Constantino; Vallada, Homero Pinto
Fonte: American Journal of Medical Genetics. Nome do evento: World Congress of Psychiatric Genetics. Unidade: FM
Assuntos: TIQUES (GENÉTICA), GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAMOS CASTILLO, J. C. et al. Candiddate genes for Tourette's: the DAT1 and 5HT1Dbeta preliminary results. American Journal of Medical Genetics. Danvers: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 24 out. 2025. , 2003
APA
Ramos Castillo, J. C., Castillo, A., Velloso, I., Miguita, K., Ekinaga, E., Correa, R., et al. (2003). Candiddate genes for Tourette's: the DAT1 and 5HT1Dbeta preliminary results. American Journal of Medical Genetics. Danvers: Faculdade de Medicina, Universidade de São Paulo.
NLM
Ramos Castillo JC, Castillo A, Velloso I, Miguita K, Ekinaga E, Correa R, Biason L, Nunes L, Castro A, Gosling F, Halpern B, Miguel EC, Vallada HP. Candiddate genes for Tourette's: the DAT1 and 5HT1Dbeta preliminary results. American Journal of Medical Genetics. 2003 ; 122B( 1): 138.[citado 2025 out. 24 ]
Vancouver
Ramos Castillo JC, Castillo A, Velloso I, Miguita K, Ekinaga E, Correa R, Biason L, Nunes L, Castro A, Gosling F, Halpern B, Miguel EC, Vallada HP. Candiddate genes for Tourette's: the DAT1 and 5HT1Dbeta preliminary results. American Journal of Medical Genetics. 2003 ; 122B( 1): 138.[citado 2025 out. 24 ]
Artigo de periodico
Disclosing the mechanisms of origin of de novo short-arm duplications of chromosome 9 (2003)
Krepischi, Ana Cristina Victorino ; Vianna-Morgante, Angela M
Fonte: American Journal of Medical Genetics. Unidade: IB
Assuntos: CROMOSSOMOS HUMANOS, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KREPISCHI, Ana Cristina Victorino e VIANNA-MORGANTE, Angela M. Disclosing the mechanisms of origin of de novo short-arm duplications of chromosome 9. American Journal of Medical Genetics, v. 117A, n. 1, p. 41-46, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.10634. Acesso em: 24 out. 2025.
APA
Krepischi, A. C. V., & Vianna-Morgante, A. M. (2003). Disclosing the mechanisms of origin of de novo short-arm duplications of chromosome 9. American Journal of Medical Genetics, 117A( 1), 41-46. doi:10.1002/ajmg.a.10634
NLM
Krepischi ACV, Vianna-Morgante AM. Disclosing the mechanisms of origin of de novo short-arm duplications of chromosome 9 [Internet]. American Journal of Medical Genetics. 2003 ; 117A( 1): 41-46.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.10634
Vancouver
Krepischi ACV, Vianna-Morgante AM. Disclosing the mechanisms of origin of de novo short-arm duplications of chromosome 9 [Internet]. American Journal of Medical Genetics. 2003 ; 117A( 1): 41-46.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.10634
Artigo de periodico
Teebi hypertelorism syndrome: additional cases (2003)
Paula, Ligiane Alves Machado; Guion-Almeida, Maria Leine
Fonte: American Journal of Medical Genetics. Unidade: HRAC
Assuntos: ANORMALIDADES MÚLTIPLAS, HIPERTELORISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PAULA, Ligiane Alves Machado e GUION-ALMEIDA, Maria Leine. Teebi hypertelorism syndrome: additional cases. American Journal of Medical Genetics, v. 117A, n. 2, p. 181-183, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.10919. Acesso em: 24 out. 2025.
APA
Paula, L. A. M., & Guion-Almeida, M. L. (2003). Teebi hypertelorism syndrome: additional cases. American Journal of Medical Genetics, 117A( 2), 181-183. doi:10.1002/ajmg.a.10919
NLM
Paula LAM, Guion-Almeida ML. Teebi hypertelorism syndrome: additional cases [Internet]. American Journal of Medical Genetics. 2003 ; 117A( 2): 181-183.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.10919
Vancouver
Paula LAM, Guion-Almeida ML. Teebi hypertelorism syndrome: additional cases [Internet]. American Journal of Medical Genetics. 2003 ; 117A( 2): 181-183.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.10919
Artigo de periodico
Newborn with malformations and a combined duplication of 9pter-q22 and 16q22-qter resulting from unbalanced segregation of a complex maternal translocation (2003)
Piram, Adriana; Ortolan, Daniela; Peres, Luiz César; Pina Neto, João Monteiro de; Riegel, Mariluce; Schinzel, Albert
Fonte: American Journal of Medical Genetics. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PIRAM, Adriana et al. Newborn with malformations and a combined duplication of 9pter-q22 and 16q22-qter resulting from unbalanced segregation of a complex maternal translocation. American Journal of Medical Genetics, v. 120A, p. 247-252, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.10004. Acesso em: 24 out. 2025.
APA
Piram, A., Ortolan, D., Peres, L. C., Pina Neto, J. M. de, Riegel, M., & Schinzel, A. (2003). Newborn with malformations and a combined duplication of 9pter-q22 and 16q22-qter resulting from unbalanced segregation of a complex maternal translocation. American Journal of Medical Genetics, 120A, 247-252. doi:10.1002/ajmg.a.10004
NLM
Piram A, Ortolan D, Peres LC, Pina Neto JM de, Riegel M, Schinzel A. Newborn with malformations and a combined duplication of 9pter-q22 and 16q22-qter resulting from unbalanced segregation of a complex maternal translocation [Internet]. American Journal of Medical Genetics. 2003 ; 120A 247-252.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.10004
Vancouver
Piram A, Ortolan D, Peres LC, Pina Neto JM de, Riegel M, Schinzel A. Newborn with malformations and a combined duplication of 9pter-q22 and 16q22-qter resulting from unbalanced segregation of a complex maternal translocation [Internet]. American Journal of Medical Genetics. 2003 ; 120A 247-252.[citado 2025 out. 24 ] Available from: https://doi.org/10.1002/ajmg.a.10004

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