Fluorescence in situ hybridization (FISH) screening for the 22q11.2 deletion in patients with clinical features of velocardiofacial syndrome but without cardiac anomalies (2007)
- Authors:
- Autor USP: COSTA, ANTONIO RICHIERI DA - HRAC
- Unidade: HRAC
- DOI: 10.1590/s1415-47572007000100006
- Subjects: INSUFICIÊNCIA VELOFARÍNGEA; DELEÇÃO DE GENES; FLUORESCÊNCIA
- Language: Português
- Imprenta:
- Source:
- Título do periódico: Genetics and Molecular Biology
- ISSN: 1415-4757
- Volume/Número/Paginação/Ano: v. 30, n. 1, p. 21-24, 2007
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by
-
ABNT
SANDRIN-GARCIA, Paula et al. Fluorescence in situ hybridization (FISH) screening for the 22q11.2 deletion in patients with clinical features of velocardiofacial syndrome but without cardiac anomalies. Genetics and Molecular Biology, v. 30, n. 1, p. 21-24, 2007Tradução . . Disponível em: https://doi.org/10.1590/s1415-47572007000100006. Acesso em: 18 set. 2024. -
APA
Sandrin-Garcia, P., Richieri-Costa, A., Tajara, E. H., Carvalho-Salles, A. B., & Fett-Conte, A. C. (2007). Fluorescence in situ hybridization (FISH) screening for the 22q11.2 deletion in patients with clinical features of velocardiofacial syndrome but without cardiac anomalies. Genetics and Molecular Biology, 30( 1), 21-24. doi:10.1590/s1415-47572007000100006 -
NLM
Sandrin-Garcia P, Richieri-Costa A, Tajara EH, Carvalho-Salles AB, Fett-Conte AC. Fluorescence in situ hybridization (FISH) screening for the 22q11.2 deletion in patients with clinical features of velocardiofacial syndrome but without cardiac anomalies [Internet]. Genetics and Molecular Biology. 2007 ; 30( 1): 21-24.[citado 2024 set. 18 ] Available from: https://doi.org/10.1590/s1415-47572007000100006 -
Vancouver
Sandrin-Garcia P, Richieri-Costa A, Tajara EH, Carvalho-Salles AB, Fett-Conte AC. Fluorescence in situ hybridization (FISH) screening for the 22q11.2 deletion in patients with clinical features of velocardiofacial syndrome but without cardiac anomalies [Internet]. Genetics and Molecular Biology. 2007 ; 30( 1): 21-24.[citado 2024 set. 18 ] Available from: https://doi.org/10.1590/s1415-47572007000100006 - Tibial hemimelia-split hand/foot syndrome, report of a brazilian family
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Informações sobre o DOI: 10.1590/s1415-47572007000100006 (Fonte: oaDOI API)
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