Pai syndrome: report of seven south american patients (2007)
- Authors:
- USP affiliated authors: ALMEIDA, MARIA LEINE GUION DE - HRAC ; COSTA, ANTONIO RICHIERI DA - HRAC
- Unidade: HRAC
- Subjects: ANORMALIDADES MÚLTIPLAS; ANORMALIDADES CRANIOFACIAIS; HIPERTELORISMO; LÁBIO FISSURADO
- Language: Inglês
- Imprenta:
- Source:
- Título: American Journal of Medical Genetics. Part A
- ISSN: 1552-4825
- Volume/Número/Paginação/Ano: v. 143A, n. 24, p. 3273-3279, Dec. 2007
-
ABNT
GUION-ALMEIDA, Maria Leine et al. Pai syndrome: report of seven south american patients. American Journal of Medical Genetics. Part A, v. 143A, n. 24, p. 3273-3279, 2007Tradução . . Disponível em: http://www3.interscience.wiley.com/cgi-bin/fulltext/116325032/PDFSTART?CRETRY=1&SRETRY=0. Acesso em: 22 jan. 2026. -
APA
Guion-Almeida, M. L., Mellado, C., Beltrán, C., & Richieri-Costa, A. (2007). Pai syndrome: report of seven south american patients. American Journal of Medical Genetics. Part A, 143A( 24), 3273-3279. Recuperado de http://www3.interscience.wiley.com/cgi-bin/fulltext/116325032/PDFSTART?CRETRY=1&SRETRY=0 -
NLM
Guion-Almeida ML, Mellado C, Beltrán C, Richieri-Costa A. Pai syndrome: report of seven south american patients [Internet]. American Journal of Medical Genetics. Part A. 2007 ; 143A( 24): 3273-3279.[citado 2026 jan. 22 ] Available from: http://www3.interscience.wiley.com/cgi-bin/fulltext/116325032/PDFSTART?CRETRY=1&SRETRY=0 -
Vancouver
Guion-Almeida ML, Mellado C, Beltrán C, Richieri-Costa A. Pai syndrome: report of seven south american patients [Internet]. American Journal of Medical Genetics. Part A. 2007 ; 143A( 24): 3273-3279.[citado 2026 jan. 22 ] Available from: http://www3.interscience.wiley.com/cgi-bin/fulltext/116325032/PDFSTART?CRETRY=1&SRETRY=0 - Conjoined twins: report of a Brazilian twin belonging to the category duplicatas incompleta, an atypical parasite twinning type
- Perfil diagnóstico clínico/genético dos óbitos intra-hospitalar, em 40 anos de atividades do HRAC-USP: dados preliminares
- Oculoauriculovertebral spectrum with radial defects: a new syndrome or an extension of the oculoauriculovertebral spectrum? Report of fourteen brazilian cases and review of the literature
- Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes
- Clinical genetic study of 144 patients with nonsyndromic hearing loss
- 22q11 Deletion Syndrome and limb anomalies: report on two brazilian patients
- Síndrome de Stickler: avaliação clínica, triagem de mutação no gene COL2A1, correlação genótipo/fenótipo e implicação para o diagnóstico
- Acro-fronto-facio-nasal dysostosis: report of a new Brazilian family
- Ectodermal dysplasia, ectrodactyly, clefting, anophthalmia/microphthalmia, and genitourinary anomalies: nosology of goltz-gorlin syndrome versus EEC syndrome
- Atypical craniofacial clefts: a syndromological approach
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas