Autosomal recessive ectodermal dysplasia, cleft lip/palate, mental retardation, and syndactyly: the Zlotogora-Ogur syndrome (1990)
- Authors:
- Autor USP: COSTA, ANTONIO RICHIERI DA - HRAC
- Unidade: HRAC
- DOI: 10.1002/ajmg.1320360420
- Subjects: FISSURA LÁBIOPALATINA; RETARDO MENTAL; ANORMALIDADES MÚLTIPLAS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American Journal of Medical Genetics
- Volume/Número/Paginação/Ano: v. 36, n. 4, p. 473-476, Aug. 1990
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
RODINI, Elaine Sbroggio de Oliveira; RICHIERI-COSTA, Antonio. Autosomal recessive ectodermal dysplasia, cleft lip/palate, mental retardation, and syndactyly: the Zlotogora-Ogur syndrome. American Journal of Medical Genetics, New York, v. 36, n. 4, p. 473-476, 1990. DOI: 10.1002/ajmg.1320360420. -
APA
Rodini, E. S. de O., & Richieri-Costa, A. (1990). Autosomal recessive ectodermal dysplasia, cleft lip/palate, mental retardation, and syndactyly: the Zlotogora-Ogur syndrome. American Journal of Medical Genetics, 36( 4), 473-476. doi:10.1002/ajmg.1320360420 -
NLM
Rodini ES de O, Richieri-Costa A. Autosomal recessive ectodermal dysplasia, cleft lip/palate, mental retardation, and syndactyly: the Zlotogora-Ogur syndrome. American Journal of Medical Genetics. 1990 ; 36( 4): 473-476. -
Vancouver
Rodini ES de O, Richieri-Costa A. Autosomal recessive ectodermal dysplasia, cleft lip/palate, mental retardation, and syndactyly: the Zlotogora-Ogur syndrome. American Journal of Medical Genetics. 1990 ; 36( 4): 473-476. - Marden-walker-like syndrome without psychomotor retardation: report of a Brazilian girl born to consaguineous parents
- Carpenter syndrome with normal intelligence: Brazilian girl born consanguineous parents
- A newly recognized autosomal dominant mandibulofacaial dysostosis (Bauru type): report on a Brazilian family
- Brief clinical report: sporadic, idiopathic MCA/MR syndrome with the tibial aplasia/femoral bifurcation field defect
- Periventricular neuronal heterotopia, oro-facio-digital anomalies, and microphthalmia: a new syndrom
- A novel heterozygous missense mutation G316D of SIX3 gene in a brazilian patient with holoprosencephaly-like phenotype and Langerhans cell histiocytosis
- Unique alterations of an ultraconserved non-coding Element in the 3′UTR of ZIC2 in holoprosencephaly
- Genetical analysis in 148 brazilian cases with holoprosencephaly
- Puretic syndrome in a Brazilian child
- Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF-β, hedgehog, and FGF signaling
Informações sobre o DOI: 10.1002/ajmg.1320360420 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas