Variable phenotypic manifestations of a K44N mutation in the TGIF gene (2008)
- Authors:
- USP affiliated author: COSTA, ANTONIO RICHIERI DA - HRAC
- School: HRAC
- DOI: 10.1016/j.braindev.2007.07.012
- Subjects: HOLOPROSENCEFALIA; GENES
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Brain & Development
- ISSN: 0387-7604
- Volume/Número/Paginação/Ano: v. 30, n. 3, p. 203-205, Mar. 2008
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
RICHIERI-COSTA, Antonio; RIBEIRO, Lucilene Arilho. Variable phenotypic manifestations of a K44N mutation in the TGIF gene. Brain & Development, Amsterdam, v. 30, n. 3, p. 203-205, 2008. Disponível em: < http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T50-4PKP4CR-1&_user=5674931&_rdoc=1&_fmt=&_orig=search&_sort=d&view=c&_version=1&_urlVersion=0&_userid=5674931&md5=4e12447c0670d7bc8406cf734844a5a7 > DOI: 10.1016/j.braindev.2007.07.012. -
APA
Richieri-Costa, A., & Ribeiro, L. A. (2008). Variable phenotypic manifestations of a K44N mutation in the TGIF gene. Brain & Development, 30( 3), 203-205. doi:10.1016/j.braindev.2007.07.012 -
NLM
Richieri-Costa A, Ribeiro LA. Variable phenotypic manifestations of a K44N mutation in the TGIF gene [Internet]. Brain & Development. 2008 ; 30( 3): 203-205.Available from: http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T50-4PKP4CR-1&_user=5674931&_rdoc=1&_fmt=&_orig=search&_sort=d&view=c&_version=1&_urlVersion=0&_userid=5674931&md5=4e12447c0670d7bc8406cf734844a5a7 -
Vancouver
Richieri-Costa A, Ribeiro LA. Variable phenotypic manifestations of a K44N mutation in the TGIF gene [Internet]. Brain & Development. 2008 ; 30( 3): 203-205.Available from: http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T50-4PKP4CR-1&_user=5674931&_rdoc=1&_fmt=&_orig=search&_sort=d&view=c&_version=1&_urlVersion=0&_userid=5674931&md5=4e12447c0670d7bc8406cf734844a5a7 - Fluorescence in situ hybridization (FISH) screening for the 22q11.2 deletion in patients with clinical features of velocardiofacial syndrome but without cardiac anomalies
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Informações sobre o DOI: 10.1016/j.braindev.2007.07.012 (Fonte: oaDOI API)
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