Tibial hemimelia: reporto on 37 new cases, clinical and gentic considerations (1987)
- Authors:
- USP affiliated authors: COSTA, ANTONIO RICHIERI DA - HRAC
- Unidades: HRAC
- DOI: 10.1002/ajmg.1320270414
- Subjects: ANORMALIDADES MÚLTIPLAS; FENÓTIPOS; GENÉTICA MÉDICA
- Language: Português
- Imprenta:
- Source:
- Título do periódico: American Journal of Medical Genetics
- Volume/Número/Paginação/Ano: v.27, n.4 , p.867-84, aug. 1987
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
RICHIERI-COSTA, A; FERRARETO, I; MASIERO, D; SILVA, C R M. Tibial hemimelia: reporto on 37 new cases, clinical and gentic considerations. American Journal of Medical Genetics, New York, v. 27, n. 4 , p. 867-84, 1987. DOI: 10.1002/ajmg.1320270414. -
APA
Richieri-Costa, A., Ferrareto, I., Masiero, D., & Silva, C. R. M. (1987). Tibial hemimelia: reporto on 37 new cases, clinical and gentic considerations. American Journal of Medical Genetics, 27( 4 ), 867-84. doi:10.1002/ajmg.1320270414 -
NLM
Richieri-Costa A, Ferrareto I, Masiero D, Silva CRM. Tibial hemimelia: reporto on 37 new cases, clinical and gentic considerations. American Journal of Medical Genetics. 1987 ;27( 4 ): 867-84. -
Vancouver
Richieri-Costa A, Ferrareto I, Masiero D, Silva CRM. Tibial hemimelia: reporto on 37 new cases, clinical and gentic considerations. American Journal of Medical Genetics. 1987 ;27( 4 ): 867-84. - Blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) and cleft lip and palate. Report of two Brazilian families
- Branchio-oto-renal (BOR) syndrome: report of a brazilian family
- Mutation in the homeodomain of the human SIX3 gene cause holoprosencephaly
- Genotype-phenotype correlation in two patients with familiar Pfeiffer syndrome
- Oculo-auriculo-vertebral complex and uncommon associated anomalies: report on 8 unrelated
- A década da linguagem - os genes começam a falar
- Macrostomia, preauricular tags, and external ophthalmoplegia: a new autosomal dominant syndrome within the oculoauriculovertebral spectrum?
- Oblique facial clefts: report on 4 Brazilian patients. Evidence for clinical variability and genetic heterogeneity
- Holoprosencephaly and holoprosencephaly-like phenotypes: review of facial and molecular findings in patients from a craniofacial hospital in Brazil
- SIX3 mutations with holoprosencephaly
Informações sobre o DOI: 10.1002/ajmg.1320270414 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
