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Artigo de periodico
ENAM gene polymorphisms associated with dental anomalies in individuals with cleft lip and palate (2024)
Oliveira, Fernanda Veronese de ; Santos, Carlos Ferreira dos ; Dionisio, Thiago José ; Neves, Lucimara Teixeira das ; Dalben, Gisele da Silva ; Ambrosio, Eloá Cristina Passucci ; Jorge, Paula Karine ; Machado, Maria Aparecida de Andrade Moreira ; Oliveira, Thais Marchini de
Source: Brazilian Journal of Oral Sciences. Unidades: FOB, HRAC
Subjects: FISSURA PALATINA, POLIMORFISMO, NUCLEOTÍDEOS, PROTEÍNAS, MATRIZ EXTRACELULAR
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ABNT
OLIVEIRA, Fernanda Veronese de et al. ENAM gene polymorphisms associated with dental anomalies in individuals with cleft lip and palate. Brazilian Journal of Oral Sciences, v. 23, 2024Tradução . . Disponível em: http://dx.doi.org/10.20396/bjos.v23i00.8671330. Acesso em: 06 out. 2024.
APA
Oliveira, F. V. de, Santos, C. F. dos, Dionisio, T. J., Neves, L. T. das, Dalben, G. da S., Ambrosio, E. C. P., et al. (2024). ENAM gene polymorphisms associated with dental anomalies in individuals with cleft lip and palate. Brazilian Journal of Oral Sciences, 23. doi:10.20396/bjos.v23i00.8671330
NLM
Oliveira FV de, Santos CF dos, Dionisio TJ, Neves LT das, Dalben G da S, Ambrosio ECP, Jorge PK, Machado MA de AM, Oliveira TM de. ENAM gene polymorphisms associated with dental anomalies in individuals with cleft lip and palate [Internet]. Brazilian Journal of Oral Sciences. 2024 ; 23[citado 2024 out. 06 ] Available from: http://dx.doi.org/10.20396/bjos.v23i00.8671330
Vancouver
Oliveira FV de, Santos CF dos, Dionisio TJ, Neves LT das, Dalben G da S, Ambrosio ECP, Jorge PK, Machado MA de AM, Oliveira TM de. ENAM gene polymorphisms associated with dental anomalies in individuals with cleft lip and palate [Internet]. Brazilian Journal of Oral Sciences. 2024 ; 23[citado 2024 out. 06 ] Available from: http://dx.doi.org/10.20396/bjos.v23i00.8671330
Artigo de periodico
Brazilian multiethnic association study of genetic variant interactions among FOS, CASP8, MMP2 and CRISPLD2 in the risk of nonsyndromic cleft lip with or without cleft palate (2023)
Machado, Renato Assis ; Oliveira, Lilianny Querino Rocha de ; Rangel, Ana Lúcia Carrinho Ayroza ; Reis, Silvia Regina de Almeida; Scariot, Rafaela ; Martelli, Daniella Reis Barbosa ; Martelli-Júnior, Hercílio ; Coletta, Ricardo Della
Source: Dentistry Journal. Unidade: HRAC
Subjects: LÁBIO FISSURADO, FISSURA PALATINA, POLIMORFISMO, EPISTEMOLOGIA GENÉTICA
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ABNT
MACHADO, Renato Assis et al. Brazilian multiethnic association study of genetic variant interactions among FOS, CASP8, MMP2 and CRISPLD2 in the risk of nonsyndromic cleft lip with or without cleft palate. Dentistry Journal, v. 11, n. Ja 2023, 2023Tradução . . Disponível em: https://doi.org/10.3390/dj11010007. Acesso em: 06 out. 2024.
APA
Machado, R. A., Oliveira, L. Q. R. de, Rangel, A. L. C. A., Reis, S. R. de A., Scariot, R., Martelli, D. R. B., et al. (2023). Brazilian multiethnic association study of genetic variant interactions among FOS, CASP8, MMP2 and CRISPLD2 in the risk of nonsyndromic cleft lip with or without cleft palate. Dentistry Journal, 11( Ja 2023). doi:10.3390/dj11010007
NLM
Machado RA, Oliveira LQR de, Rangel ALCA, Reis SR de A, Scariot R, Martelli DRB, Martelli-Júnior H, Coletta RD. Brazilian multiethnic association study of genetic variant interactions among FOS, CASP8, MMP2 and CRISPLD2 in the risk of nonsyndromic cleft lip with or without cleft palate [Internet]. Dentistry Journal. 2023 ; 11( Ja 2023):[citado 2024 out. 06 ] Available from: https://doi.org/10.3390/dj11010007
Vancouver
Machado RA, Oliveira LQR de, Rangel ALCA, Reis SR de A, Scariot R, Martelli DRB, Martelli-Júnior H, Coletta RD. Brazilian multiethnic association study of genetic variant interactions among FOS, CASP8, MMP2 and CRISPLD2 in the risk of nonsyndromic cleft lip with or without cleft palate [Internet]. Dentistry Journal. 2023 ; 11( Ja 2023):[citado 2024 out. 06 ] Available from: https://doi.org/10.3390/dj11010007
Artigo de periodico
Machine learning in prediction of genetic risk of nonsyndromic oral clefts in the Brazilian population (2021)
Machado, Renato Assis ; Silva, Carolina de Oliveira; Martelli Júnior, Hercílio ; Neves, Lucimara Teixeira das ; Coletta, Ricardo D.
Source: Clinical Oral Investigations. Unidades: FOB, HRAC
Subjects: FISSURA LÁBIOPALATINA, POLIMORFISMO, APRENDIZADO COMPUTACIONAL, ACONSELHAMENTO GENÉTICO
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ABNT
MACHADO, Renato Assis et al. Machine learning in prediction of genetic risk of nonsyndromic oral clefts in the Brazilian population. Clinical Oral Investigations, v. 25, n. 3, p. 1273-1280, 2021Tradução . . Disponível em: https://doi.org/10.1007/s00784-020-03433-y. Acesso em: 06 out. 2024.
APA
Machado, R. A., Silva, C. de O., Martelli Júnior, H., Neves, L. T. das, & Coletta, R. D. (2021). Machine learning in prediction of genetic risk of nonsyndromic oral clefts in the Brazilian population. Clinical Oral Investigations, 25( 3), 1273-1280. doi:10.1007/s00784-020-03433-y
NLM
Machado RA, Silva C de O, Martelli Júnior H, Neves LT das, Coletta RD. Machine learning in prediction of genetic risk of nonsyndromic oral clefts in the Brazilian population [Internet]. Clinical Oral Investigations. 2021 ; 25( 3): 1273-1280.[citado 2024 out. 06 ] Available from: https://doi.org/10.1007/s00784-020-03433-y
Vancouver
Machado RA, Silva C de O, Martelli Júnior H, Neves LT das, Coletta RD. Machine learning in prediction of genetic risk of nonsyndromic oral clefts in the Brazilian population [Internet]. Clinical Oral Investigations. 2021 ; 25( 3): 1273-1280.[citado 2024 out. 06 ] Available from: https://doi.org/10.1007/s00784-020-03433-y
Artigo de periodico
Association between MSX1 rs12532 polymorphism with nonsyndromic unilateral complete cleft lip and palate and tooth agenesis (2020)
Lancia, Melissa; Machado, Renato Assis; Dionisio, Thiago José ; Garib, Daniela Gamba ; Santos, Carlos Ferreira dos ; Coletta, Ricardo D. ; Neves, Lucimara Teixeira das
Source: Archives of Oral Biology. Unidades: FOB, HRAC
Subjects: POLIMORFISMO, FISSURA LÁBIOPALATINA, AGENESIA, FATORES DE RISCO
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ABNT
LANCIA, Melissa et al. Association between MSX1 rs12532 polymorphism with nonsyndromic unilateral complete cleft lip and palate and tooth agenesis. Archives of Oral Biology, v. 109, n. Ja 2020, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.archoralbio.2019.104556. Acesso em: 06 out. 2024.
APA
Lancia, M., Machado, R. A., Dionisio, T. J., Garib, D. G., Santos, C. F. dos, Coletta, R. D., & Neves, L. T. das. (2020). Association between MSX1 rs12532 polymorphism with nonsyndromic unilateral complete cleft lip and palate and tooth agenesis. Archives of Oral Biology, 109( Ja 2020). doi:10.1016/j.archoralbio.2019.104556
NLM
Lancia M, Machado RA, Dionisio TJ, Garib DG, Santos CF dos, Coletta RD, Neves LT das. Association between MSX1 rs12532 polymorphism with nonsyndromic unilateral complete cleft lip and palate and tooth agenesis [Internet]. Archives of Oral Biology. 2020 ; 109( Ja 2020):[citado 2024 out. 06 ] Available from: https://doi.org/10.1016/j.archoralbio.2019.104556
Vancouver
Lancia M, Machado RA, Dionisio TJ, Garib DG, Santos CF dos, Coletta RD, Neves LT das. Association between MSX1 rs12532 polymorphism with nonsyndromic unilateral complete cleft lip and palate and tooth agenesis [Internet]. Archives of Oral Biology. 2020 ; 109( Ja 2020):[citado 2024 out. 06 ] Available from: https://doi.org/10.1016/j.archoralbio.2019.104556
Trabalho de evento-resumo
Genetic predisposition in non-syndromic cleft lip and palate: pilot study of polymorphic variants in MMP-3 gene (2019)
Silva, Carolina Maia; Olano-Dextre, Tulio Lorenzo; Queiroz, Thaís Bernardes de; Pereira, Maria Carolina de Moraes; Mateo-Castillo, José Francisco ; Gonçales, Andréa Guedes Barreto ; Neves, Lucimara Teixeira das
Source: Anais. Conference titles: Workshop de Genética. Unidades: FOB, HRAC, HRACF
Subjects: FISSURA LÁBIOPALATINA, HEREDITARIEDADE, POLIMORFISMO
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ABNT
SILVA, Carolina Maia et al. Genetic predisposition in non-syndromic cleft lip and palate: pilot study of polymorphic variants in MMP-3 gene. 2019, Anais.. Botucatu: Instituto de Biociências de Botucatu - UNESP, 2019. Disponível em: https://repositorio.usp.br/directbitstream/88785b13-54ed-45cb-8ea3-f2e7ce179cc1/3088541.pdf. Acesso em: 06 out. 2024.
APA
Silva, C. M., Olano-Dextre, T. L., Queiroz, T. B. de, Pereira, M. C. de M., Mateo-Castillo, J. F., Gonçales, A. G. B., & Neves, L. T. das. (2019). Genetic predisposition in non-syndromic cleft lip and palate: pilot study of polymorphic variants in MMP-3 gene. In Anais. Botucatu: Instituto de Biociências de Botucatu - UNESP. Recuperado de https://repositorio.usp.br/directbitstream/88785b13-54ed-45cb-8ea3-f2e7ce179cc1/3088541.pdf
NLM
Silva CM, Olano-Dextre TL, Queiroz TB de, Pereira MC de M, Mateo-Castillo JF, Gonçales AGB, Neves LT das. Genetic predisposition in non-syndromic cleft lip and palate: pilot study of polymorphic variants in MMP-3 gene [Internet]. Anais. 2019 ;[citado 2024 out. 06 ] Available from: https://repositorio.usp.br/directbitstream/88785b13-54ed-45cb-8ea3-f2e7ce179cc1/3088541.pdf
Vancouver
Silva CM, Olano-Dextre TL, Queiroz TB de, Pereira MC de M, Mateo-Castillo JF, Gonçales AGB, Neves LT das. Genetic predisposition in non-syndromic cleft lip and palate: pilot study of polymorphic variants in MMP-3 gene [Internet]. Anais. 2019 ;[citado 2024 out. 06 ] Available from: https://repositorio.usp.br/directbitstream/88785b13-54ed-45cb-8ea3-f2e7ce179cc1/3088541.pdf
Trabalho de evento-resumo
Polymorphic variants in the MMP-2 gene and the non-syndromic cleft lip and palate: a pilot study of their possible association (2019)
Queiroz, Thaís Bernardes de; Olano-Dextre, Tulio Lorenzo; Silva, Carolina Maia; Pereira, Maria Carolina de Moraes; Gonçales, Andréa Guedes Barreto ; Mateo-Castillo, José Francisco ; Neves, Lucimara Teixeira das
Source: Anais. Conference titles: Workshop de Genética. Unidades: FOB, HRAC, HRACF
Subjects: METALOPROTEINASES, FISSURA LÁBIOPALATINA, POLIMORFISMO
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ABNT
QUEIROZ, Thaís Bernardes de et al. Polymorphic variants in the MMP-2 gene and the non-syndromic cleft lip and palate: a pilot study of their possible association. 2019, Anais.. Botucatu: Instituto de Biociências de Botucatu - UNESP, 2019. Disponível em: https://repositorio.usp.br/directbitstream/0b00e881-863e-4db0-82c4-d1a8a6094a6b/3088547.pdf. Acesso em: 06 out. 2024.
APA
Queiroz, T. B. de, Olano-Dextre, T. L., Silva, C. M., Pereira, M. C. de M., Gonçales, A. G. B., Mateo-Castillo, J. F., & Neves, L. T. das. (2019). Polymorphic variants in the MMP-2 gene and the non-syndromic cleft lip and palate: a pilot study of their possible association. In Anais. Botucatu: Instituto de Biociências de Botucatu - UNESP. Recuperado de https://repositorio.usp.br/directbitstream/0b00e881-863e-4db0-82c4-d1a8a6094a6b/3088547.pdf
NLM
Queiroz TB de, Olano-Dextre TL, Silva CM, Pereira MC de M, Gonçales AGB, Mateo-Castillo JF, Neves LT das. Polymorphic variants in the MMP-2 gene and the non-syndromic cleft lip and palate: a pilot study of their possible association [Internet]. Anais. 2019 ;[citado 2024 out. 06 ] Available from: https://repositorio.usp.br/directbitstream/0b00e881-863e-4db0-82c4-d1a8a6094a6b/3088547.pdf
Vancouver
Queiroz TB de, Olano-Dextre TL, Silva CM, Pereira MC de M, Gonçales AGB, Mateo-Castillo JF, Neves LT das. Polymorphic variants in the MMP-2 gene and the non-syndromic cleft lip and palate: a pilot study of their possible association [Internet]. Anais. 2019 ;[citado 2024 out. 06 ] Available from: https://repositorio.usp.br/directbitstream/0b00e881-863e-4db0-82c4-d1a8a6094a6b/3088547.pdf
Trabalho de evento
Genetic susceptibility to chronic apical periodontitis in individuals withcleft lip and/or palate (2017)
Olano-Dextre, Tulio Lorenzo; Dionísio, Thiago José; Pinto, Lidiane de Castro; Nishiyama, Celso Kenji; Santos, Carlos Ferreira dos; Duarte, Marco Antonio Hungaro; Neves, Lucimara Teixeira das
Source: Anais. Conference titles: Simpósio Internacional de Fissuras Orofaciais e Anomalias Relacionadas. Unidades: FOB, HRAC
Subjects: PERIODONTITE, POLIMORFISMO, ENDODONTIA, FISSURA LÁBIOPALATINA
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ABNT
OLANO-DEXTRE, Tulio Lorenzo et al. Genetic susceptibility to chronic apical periodontitis in individuals withcleft lip and/or palate. 2017, Anais.. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, 2017. Disponível em: https://repositorio.usp.br/directbitstream/36eedce8-5286-4e69-be7e-1e8c5e4d6d73/2940087.pdf. Acesso em: 06 out. 2024.
APA
Olano-Dextre, T. L., Dionísio, T. J., Pinto, L. de C., Nishiyama, C. K., Santos, C. F. dos, Duarte, M. A. H., & Neves, L. T. das. (2017). Genetic susceptibility to chronic apical periodontitis in individuals withcleft lip and/or palate. In Anais. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/36eedce8-5286-4e69-be7e-1e8c5e4d6d73/2940087.pdf
NLM
Olano-Dextre TL, Dionísio TJ, Pinto L de C, Nishiyama CK, Santos CF dos, Duarte MAH, Neves LT das. Genetic susceptibility to chronic apical periodontitis in individuals withcleft lip and/or palate [Internet]. Anais. 2017 ;[citado 2024 out. 06 ] Available from: https://repositorio.usp.br/directbitstream/36eedce8-5286-4e69-be7e-1e8c5e4d6d73/2940087.pdf
Vancouver
Olano-Dextre TL, Dionísio TJ, Pinto L de C, Nishiyama CK, Santos CF dos, Duarte MAH, Neves LT das. Genetic susceptibility to chronic apical periodontitis in individuals withcleft lip and/or palate [Internet]. Anais. 2017 ;[citado 2024 out. 06 ] Available from: https://repositorio.usp.br/directbitstream/36eedce8-5286-4e69-be7e-1e8c5e4d6d73/2940087.pdf
Dissertação (Mestrado)
Análise dos polimorfismos C677T e A1298C do gene MTHFR e a correlação dos micronutrientes em mães de indivíduos com fissura de lábio/palato (2013)
Viana, Camila Saramelo; Bicudo, Lucilene Arilho Ribeiro (Orientador)
Unidade: HRAC
Subjects: GENÉTICA, FISSURA LÁBIOPALATINA, POLIMORFISMO
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ABNT
VIANA, Camila Saramelo. Análise dos polimorfismos C677T e A1298C do gene MTHFR e a correlação dos micronutrientes em mães de indivíduos com fissura de lábio/palato. 2013. Dissertação (Mestrado) – Universidade de São Paulo, Bauru, 2013. Disponível em: http://www.teses.usp.br/teses/disponiveis/61/61132/tde-12112013-151436/. Acesso em: 06 out. 2024.
APA
Viana, C. S. (2013). Análise dos polimorfismos C677T e A1298C do gene MTHFR e a correlação dos micronutrientes em mães de indivíduos com fissura de lábio/palato (Dissertação (Mestrado). Universidade de São Paulo, Bauru. Recuperado de http://www.teses.usp.br/teses/disponiveis/61/61132/tde-12112013-151436/
NLM
Viana CS. Análise dos polimorfismos C677T e A1298C do gene MTHFR e a correlação dos micronutrientes em mães de indivíduos com fissura de lábio/palato [Internet]. 2013 ;[citado 2024 out. 06 ] Available from: http://www.teses.usp.br/teses/disponiveis/61/61132/tde-12112013-151436/
Vancouver
Viana CS. Análise dos polimorfismos C677T e A1298C do gene MTHFR e a correlação dos micronutrientes em mães de indivíduos com fissura de lábio/palato [Internet]. 2013 ;[citado 2024 out. 06 ] Available from: http://www.teses.usp.br/teses/disponiveis/61/61132/tde-12112013-151436/
Artigo de periodico
Comparison of mutation findings in ZIC2 between microform and classical holoprosencephaly in a Brazilian cohort (2012)
Ribeiro, Lucilene Arilho; Roessler, Erich; Hu, Ping; Pineda-Alvarez, Daniel E.; Zhou, Nan; Jones, MaryPat; Chandrasekharappa, Settara; Richieri-Costa, Antonio ; Muenke, Maximilian
Source: Birth Defects Research. Part A, Clinical and Molecular Teratology.. Unidade: HRAC
Subjects: HOLOPROSENCEFALIA, POLIMORFISMO, MUTAÇÃO GENÉTICA
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ABNT
RIBEIRO, Lucilene Arilho et al. Comparison of mutation findings in ZIC2 between microform and classical holoprosencephaly in a Brazilian cohort. Birth Defects Research. Part A, Clinical and Molecular Teratology., v. No 2012, n. 11, p. 912-917, 2012Tradução . . Disponível em: https://doi.org/10.1002/bdra.23047. Acesso em: 06 out. 2024.
APA
Ribeiro, L. A., Roessler, E., Hu, P., Pineda-Alvarez, D. E., Zhou, N., Jones, M. P., et al. (2012). Comparison of mutation findings in ZIC2 between microform and classical holoprosencephaly in a Brazilian cohort. Birth Defects Research. Part A, Clinical and Molecular Teratology., No 2012( 11), 912-917. doi:10.1002/bdra.23047
NLM
Ribeiro LA, Roessler E, Hu P, Pineda-Alvarez DE, Zhou N, Jones MP, Chandrasekharappa S, Richieri-Costa A, Muenke M. Comparison of mutation findings in ZIC2 between microform and classical holoprosencephaly in a Brazilian cohort [Internet]. Birth Defects Research. Part A, Clinical and Molecular Teratology. 2012 ; No 2012( 11): 912-917.[citado 2024 out. 06 ] Available from: https://doi.org/10.1002/bdra.23047
Vancouver
Ribeiro LA, Roessler E, Hu P, Pineda-Alvarez DE, Zhou N, Jones MP, Chandrasekharappa S, Richieri-Costa A, Muenke M. Comparison of mutation findings in ZIC2 between microform and classical holoprosencephaly in a Brazilian cohort [Internet]. Birth Defects Research. Part A, Clinical and Molecular Teratology. 2012 ; No 2012( 11): 912-917.[citado 2024 out. 06 ] Available from: https://doi.org/10.1002/bdra.23047
Artigo de periodico
Sonic hedgehog (SHH) mutation in patients within the spectrum of holoprosencephaly (2010)
Bertolacini, Claudia Danielli Pereira; Richieri-Costa, Antonio; Ribeiro-Bicudo, Lucilene Arilho
Source: Brain & Development. Unidade: HRAC
Subjects: MUTAÇÃO GENÉTICA, POLIMORFISMO, HOLOPROSENCEFALIA
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ABNT
BERTOLACINI, Claudia Danielli Pereira e RICHIERI-COSTA, Antonio e RIBEIRO-BICUDO, Lucilene Arilho. Sonic hedgehog (SHH) mutation in patients within the spectrum of holoprosencephaly. Brain & Development, v. 32, n. 3, p. 217-222, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.braindev.2009.02.014. Acesso em: 06 out. 2024.
APA
Bertolacini, C. D. P., Richieri-Costa, A., & Ribeiro-Bicudo, L. A. (2010). Sonic hedgehog (SHH) mutation in patients within the spectrum of holoprosencephaly. Brain & Development, 32( 3), 217-222. doi:10.1016/j.braindev.2009.02.014
NLM
Bertolacini CDP, Richieri-Costa A, Ribeiro-Bicudo LA. Sonic hedgehog (SHH) mutation in patients within the spectrum of holoprosencephaly [Internet]. Brain & Development. 2010 ; 32( 3): 217-222.[citado 2024 out. 06 ] Available from: https://doi.org/10.1016/j.braindev.2009.02.014
Vancouver
Bertolacini CDP, Richieri-Costa A, Ribeiro-Bicudo LA. Sonic hedgehog (SHH) mutation in patients within the spectrum of holoprosencephaly [Internet]. Brain & Development. 2010 ; 32( 3): 217-222.[citado 2024 out. 06 ] Available from: https://doi.org/10.1016/j.braindev.2009.02.014
Artigo de periodico
Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene? (1997)
Passos-Bueno, Maria Rita ; Sertié, Andréa Laurato; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics. Unidades: IB, HRAC
Subjects: SÍNDROMES OROFACIODIGITAIS, MUTAÇÃO, POLIMORFISMO
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ABNT
PASSOS-BUENO, Maria Rita e SERTIÉ, Andréa Laurato e RICHIERI-COSTA, Antonio. Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene?. American Journal of Medical Genetics, v. 71, n. 2, p. 243-245, 1997Tradução . . Disponível em: https://doi.org/10.1002/(sici)1096-8628(19970808)71:2%3C243::aid-ajmg27%3E3.0.co;2-d. Acesso em: 06 out. 2024.
APA
Passos-Bueno, M. R., Sertié, A. L., & Richieri-Costa, A. (1997). Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene? American Journal of Medical Genetics, 71( 2), 243-245. doi:10.1002/(sici)1096-8628(19970808)71:2%3C243::aid-ajmg27%3E3.0.co;2-d
NLM
Passos-Bueno MR, Sertié AL, Richieri-Costa A. Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene? [Internet]. American Journal of Medical Genetics. 1997 ; 71( 2): 243-245.[citado 2024 out. 06 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19970808)71:2%3C243::aid-ajmg27%3E3.0.co;2-d
Vancouver
Passos-Bueno MR, Sertié AL, Richieri-Costa A. Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene? [Internet]. American Journal of Medical Genetics. 1997 ; 71( 2): 243-245.[citado 2024 out. 06 ] Available from: https://doi.org/10.1002/(sici)1096-8628(19970808)71:2%3C243::aid-ajmg27%3E3.0.co;2-d

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