A microduplication of 5p15.33 reveals CLPTM1L as a candidate gene for cleft lip and palate (2013)
- Authors:
- USP affiliated authors: BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; BERTOLA, DÉBORA ROMEO - IB ; ROSENBERG, CARLA - IB
- Unidade: IB
- DOI: 10.1016/j.ejmg.2013.01.002
- Subjects: FISSURA LÁBIOPALATINA; MALFORMAÇÕES; DOENÇAS GENÉTICAS
- Language: Inglês
- Imprenta:
- Publisher place: Issy Les Mouleneaux
- Date published: 2013
- Source:
- Título do periódico: European Journal of Medical Genetics
- ISSN: 1769-7212
- Volume/Número/Paginação/Ano: v. 56, n. 4, p. 222-225, Apr. 2013
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
IZZO, Giselle; FREITAS, Erika L; KREPISCHI, Ana Cristina V; et al. A microduplication of 5p15.33 reveals CLPTM1L as a candidate gene for cleft lip and palate. European Journal of Medical Genetics, Issy Les Mouleneaux, v. 56, n. 4, p. 222-225, 2013. Disponível em: < http://dx.doi.org/10.1016/j.ejmg.2013.01.002 > DOI: 10.1016/j.ejmg.2013.01.002. -
APA
Izzo, G., Freitas, E. L., Krepischi, A. C. V., Pearson, P. L., Vasques, L. R., Passos-Bueno, M. R., et al. (2013). A microduplication of 5p15.33 reveals CLPTM1L as a candidate gene for cleft lip and palate. European Journal of Medical Genetics, 56( 4), 222-225. doi:10.1016/j.ejmg.2013.01.002 -
NLM
Izzo G, Freitas EL, Krepischi ACV, Pearson PL, Vasques LR, Passos-Bueno MR, Bertola DR, Rosenberg C. A microduplication of 5p15.33 reveals CLPTM1L as a candidate gene for cleft lip and palate [Internet]. European Journal of Medical Genetics. 2013 ; 56( 4): 222-225.Available from: http://dx.doi.org/10.1016/j.ejmg.2013.01.002 -
Vancouver
Izzo G, Freitas EL, Krepischi ACV, Pearson PL, Vasques LR, Passos-Bueno MR, Bertola DR, Rosenberg C. A microduplication of 5p15.33 reveals CLPTM1L as a candidate gene for cleft lip and palate [Internet]. European Journal of Medical Genetics. 2013 ; 56( 4): 222-225.Available from: http://dx.doi.org/10.1016/j.ejmg.2013.01.002 - Deletion 5q12: delineation of a phenotype including mental retardation and ocular defects
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Informações sobre o DOI: 10.1016/j.ejmg.2013.01.002 (Fonte: oaDOI API)
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