Clinical and genetic study on 356 Brazilian patients with a distinct phenotype of cleft lip and palate without alveolar ridge involvement (2014)
- Authors:
- USP affiliated authors: ALVAREZ, CAMILA WENCESLAU - HRAC ; ALMEIDA, MARIA LEINE GUION DE - HRAC ; COSTA, ANTONIO RICHIERI DA - HRAC
- Unidade: HRAC
- DOI: 10.1016/j.jcms.2014.08.007
- Subjects: FISSURA LÁBIOPALATINA; FENÓTIPOS; REBORDO ALVEOLAR
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of Cranio-Maxillo-Facial Surgery
- ISSN: 1010-5182
- Volume/Número/Paginação/Ano: v. 42, n. 8, p. 1952-1957, Dec. 2014
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
ALVAREZ, Camila Wenceslau e GUION-ALMEIDA, Maria Leine e RICHIERI-COSTA, Antonio. Clinical and genetic study on 356 Brazilian patients with a distinct phenotype of cleft lip and palate without alveolar ridge involvement. Journal of Cranio-Maxillo-Facial Surgery, v. 42, n. 8, p. 1952-1957, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.jcms.2014.08.007. Acesso em: 23 abr. 2024. -
APA
Alvarez, C. W., Guion-Almeida, M. L., & Richieri-Costa, A. (2014). Clinical and genetic study on 356 Brazilian patients with a distinct phenotype of cleft lip and palate without alveolar ridge involvement. Journal of Cranio-Maxillo-Facial Surgery, 42( 8), 1952-1957. doi:10.1016/j.jcms.2014.08.007 -
NLM
Alvarez CW, Guion-Almeida ML, Richieri-Costa A. Clinical and genetic study on 356 Brazilian patients with a distinct phenotype of cleft lip and palate without alveolar ridge involvement [Internet]. Journal of Cranio-Maxillo-Facial Surgery. 2014 ; 42( 8): 1952-1957.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1016/j.jcms.2014.08.007 -
Vancouver
Alvarez CW, Guion-Almeida ML, Richieri-Costa A. Clinical and genetic study on 356 Brazilian patients with a distinct phenotype of cleft lip and palate without alveolar ridge involvement [Internet]. Journal of Cranio-Maxillo-Facial Surgery. 2014 ; 42( 8): 1952-1957.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1016/j.jcms.2014.08.007 - About Cuddapah et al.: Paper Entitled “IRF6 Sequencing in Interrupted Clefting” [Carta]
- Cleft lip with cleft palate without alveolar arch involvement: a clinical and genetic study
- Disostose fronto-nasal: aspectos clínicos e genéticos
- Pai syndrome: report of seven south american patients
- Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes
- Oral teratoma, dextrocardia, and congenital heart defect: a nonrandom association or serendipity?
- Nonsyndromic alar clefts: report of five brazilian patients
- Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies
- Mental retardation, structural anomalies of the central nervous system, anophthalmia and abnormal nares: a new MCA/MR syndrome of unknown cause
- O serviço de genética clínica no HRAC/USP
Informações sobre o DOI: 10.1016/j.jcms.2014.08.007 (Fonte: oaDOI API)
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