Ectodermal dysplasia/ectrodactyly in monozygotic female twins, report of a case: review and comments on the ectodermal dysplasia/ectrodactyly (cleft lip/palate) syndromes (1986)
- Authors:
- Autor USP: COSTA, ANTONIO RICHIERI DA - HRAC
- Unidade: HRAC
- Subjects: GÊMEOS; DISPLASIA ECTODÉRMICA; FISSURA LÁBIOPALATINA; DOENÇAS GENÉTICAS
- Language: Inglês
- Imprenta:
- Publisher place: Ribeirão Preto
- Date published: 1986
- Source:
- Título: Revista Brasileira de Genética
- Volume/Número/Paginação/Ano: v. 9, n. 2, p. 349-374, June 1986
-
ABNT
RICHIERI-COSTA, Antonio et al. Ectodermal dysplasia/ectrodactyly in monozygotic female twins, report of a case: review and comments on the ectodermal dysplasia/ectrodactyly (cleft lip/palate) syndromes. Revista Brasileira de Genética, v. 9, n. 2, p. 349-374, 1986Tradução . . Acesso em: 28 jan. 2026. -
APA
Richieri-Costa, A., Moraes, S. A. de V., Ferrareto, I., & Masiero, D. (1986). Ectodermal dysplasia/ectrodactyly in monozygotic female twins, report of a case: review and comments on the ectodermal dysplasia/ectrodactyly (cleft lip/palate) syndromes. Revista Brasileira de Genética, 9( 2), 349-374. -
NLM
Richieri-Costa A, Moraes SA de V, Ferrareto I, Masiero D. Ectodermal dysplasia/ectrodactyly in monozygotic female twins, report of a case: review and comments on the ectodermal dysplasia/ectrodactyly (cleft lip/palate) syndromes. Revista Brasileira de Genética. 1986 ; 9( 2): 349-374.[citado 2026 jan. 28 ] -
Vancouver
Richieri-Costa A, Moraes SA de V, Ferrareto I, Masiero D. Ectodermal dysplasia/ectrodactyly in monozygotic female twins, report of a case: review and comments on the ectodermal dysplasia/ectrodactyly (cleft lip/palate) syndromes. Revista Brasileira de Genética. 1986 ; 9( 2): 349-374.[citado 2026 jan. 28 ] - Autosomal recessive blepharoptosis, cleft lip/palate, dental anomalies, and ectrodactyly
- Humeroradial/multiple synostosis syndrome in a Brazilian child with consanguineous parents: a new multiple synostosis syndrome?
- "New" autosomal-dominant infantile sensorineural non-progressive high-frequency hearing loss: report on a Brazilian family
- Down Syndrome in diverse populations
- Oblique facial clefts: report on 4 Brazilian patients. Evidence for clinical variability and genetic heterogeneity
- Autosomal recessive anophthalmia with multiple congenital abnormalities: type Waardenburg [Brief clinical report]
- Aspectos da fluência em tarefa de narrativa oral na síndrome del22q11.2
- 22q11.2 deletion syndrome in diverse populations
- Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous cases
- Single median maxillary central incisor, hypophyseal tumor, and SHH mutation
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
