Alobar holoprosencephaly in 2 sibs: an autosomal recessive type? (2009)
- Authors:
- USP affiliated authors: COSTA, ANTONIO RICHIERI DA - HRAC ; ALMEIDA, MARIA LEINE GUION DE - HRAC
- Unidade: HRAC
- Subjects: HOLOPROSENCEFALIA; IRMÃOS; MUTAÇÃO GENÉTICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Anais
- Conference titles: International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies: Cleft and craniofacial care experience, evolution and innovation
-
ABNT
RICHIERI-COSTA, Antonio et al. Alobar holoprosencephaly in 2 sibs: an autosomal recessive type? 2009, Anais.. Fortaleza: SOBRAPAR, 2009. Disponível em: https://repositorio.usp.br/directbitstream/6a4a7383-730d-4fff-9892-d05bc3f24197/3100185.pdf. Acesso em: 25 fev. 2026. -
APA
Richieri-Costa, A., Zechi-Ceide, R. M., Guion-Almeida, M. L., & Ribeiro, L. A. (2009). Alobar holoprosencephaly in 2 sibs: an autosomal recessive type? In Anais. Fortaleza: SOBRAPAR. Recuperado de https://repositorio.usp.br/directbitstream/6a4a7383-730d-4fff-9892-d05bc3f24197/3100185.pdf -
NLM
Richieri-Costa A, Zechi-Ceide RM, Guion-Almeida ML, Ribeiro LA. Alobar holoprosencephaly in 2 sibs: an autosomal recessive type? [Internet]. Anais. 2009 ;[citado 2026 fev. 25 ] Available from: https://repositorio.usp.br/directbitstream/6a4a7383-730d-4fff-9892-d05bc3f24197/3100185.pdf -
Vancouver
Richieri-Costa A, Zechi-Ceide RM, Guion-Almeida ML, Ribeiro LA. Alobar holoprosencephaly in 2 sibs: an autosomal recessive type? [Internet]. Anais. 2009 ;[citado 2026 fev. 25 ] Available from: https://repositorio.usp.br/directbitstream/6a4a7383-730d-4fff-9892-d05bc3f24197/3100185.pdf - Newly recognized autosomal recessive MCA/MR/overgrowth syndrome
- Severe midline craniofacial anomalies: overlap with Pai syndrome
- O serviço de genética clínica no HRAC/USP
- Oral teratoma, dextrocardia, and congenital heart defect: a nonrandom association or serendipity?
- Nonsyndromic alar clefts: report of five brazilian patients
- Mental retardation, structural anomalies of the central nervous system, anophthalmia and abnormal nares: a new MCA/MR syndrome of unknown cause
- Acro-fronto-facio-nasal dysostosis: report of a new Brazilian family
- Pai syndrome: report of seven south american patients
- Conjoined twins: report of a Brazilian twin belonging to the category duplicatas incompleta, an atypical parasite twinning type
- Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes
Download do texto completo
| Tipo | Nome | Link | |
|---|---|---|---|
 |
3100185.pdf |
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
