Ectodermal dysplasia, ectrodactyly, clefting, anophthalmia/microphthalmia, and genitourinary anomalies: nosology of goltz-gorlin syndrome versus EEC syndrome (1992)
- Authors:
- USP affiliated authors: ALMEIDA, MARIA LEINE GUION DE - HRAC ; COSTA, ANTONIO RICHIERI DA - HRAC
- Unidade: HRAC
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título: American Journal of Medical Genetics
- Volume/Número/Paginação/Ano: v. 42, n. 3, p. 276-280, Feb. 1992
-
ABNT
RODINI, E S O et al. Ectodermal dysplasia, ectrodactyly, clefting, anophthalmia/microphthalmia, and genitourinary anomalies: nosology of goltz-gorlin syndrome versus EEC syndrome. American Journal of Medical Genetics, v. 42, n. 3, p. 276-280, 1992Tradução . . Acesso em: 11 mar. 2026. -
APA
Rodini, E. S. O., Nardi, A., Guion-Almeida, M. L., & Richieri-Costa, A. (1992). Ectodermal dysplasia, ectrodactyly, clefting, anophthalmia/microphthalmia, and genitourinary anomalies: nosology of goltz-gorlin syndrome versus EEC syndrome. American Journal of Medical Genetics, 42( 3), 276-280. -
NLM
Rodini ESO, Nardi A, Guion-Almeida ML, Richieri-Costa A. Ectodermal dysplasia, ectrodactyly, clefting, anophthalmia/microphthalmia, and genitourinary anomalies: nosology of goltz-gorlin syndrome versus EEC syndrome. American Journal of Medical Genetics. 1992 ; 42( 3): 276-280.[citado 2026 mar. 11 ] -
Vancouver
Rodini ESO, Nardi A, Guion-Almeida ML, Richieri-Costa A. Ectodermal dysplasia, ectrodactyly, clefting, anophthalmia/microphthalmia, and genitourinary anomalies: nosology of goltz-gorlin syndrome versus EEC syndrome. American Journal of Medical Genetics. 1992 ; 42( 3): 276-280.[citado 2026 mar. 11 ] - 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
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
