Ulnar ray a/hypoplasia: evidence for a developmental field defect on the basis of genetic heterogeneity. Report of three Brazilian families (1986)
- Authors:
- Autor USP: COSTA, ANTONIO RICHIERI DA - HRAC
- Unidade: HRAC
- DOI: 10.1002/ajmg.1320250624
- Subjects: HETEROGENEIDADE; ANORMALIDADES CONGÊNITAS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American Journal of Medical Genetics Supplement
- Volume/Número/Paginação/Ano: v. 24, supplement 2, p. 195-206, Aug. 1986
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
RICHIERI-COSTA, Antonio e OPITZ, John M. Ulnar ray a/hypoplasia: evidence for a developmental field defect on the basis of genetic heterogeneity. Report of three Brazilian families. American Journal of Medical Genetics Supplement, v. 24, p. 195-206, 1986Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320250624. Acesso em: 25 abr. 2024. -
APA
Richieri-Costa, A., & Opitz, J. M. (1986). Ulnar ray a/hypoplasia: evidence for a developmental field defect on the basis of genetic heterogeneity. Report of three Brazilian families. American Journal of Medical Genetics Supplement, 24, 195-206. doi:10.1002/ajmg.1320250624 -
NLM
Richieri-Costa A, Opitz JM. Ulnar ray a/hypoplasia: evidence for a developmental field defect on the basis of genetic heterogeneity. Report of three Brazilian families [Internet]. American Journal of Medical Genetics Supplement. 1986 ; 24 195-206.[citado 2024 abr. 25 ] Available from: https://doi.org/10.1002/ajmg.1320250624 -
Vancouver
Richieri-Costa A, Opitz JM. Ulnar ray a/hypoplasia: evidence for a developmental field defect on the basis of genetic heterogeneity. Report of three Brazilian families [Internet]. American Journal of Medical Genetics Supplement. 1986 ; 24 195-206.[citado 2024 abr. 25 ] Available from: https://doi.org/10.1002/ajmg.1320250624 - Tibial hemimelia-split hand/foot syndrome, report of a brazilian family
- Tibial hemimelia: report of a new brazilian family an overview
- Atypical craniofacial clefts: a syndromological approach
- A década da linguagem: os genes começam a falar
- Estudo genético-clínico de 144 pacientes portadores de deficiência auditiva não sindrômica
- Atypical interhemispheric fusion with a cebocephalic-like functional single nostril nose and a novel SHH mutation
- Perfil audiológico de indivíduos portadores da síndrome de Goldenhar
- Identity by descent and candidate gene mapping of Richieri-Costa and Pereira syndrome
- Variable phenotypic manifestations of a K44N mutation in the TGIF gene
- PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI
Informações sobre o DOI: 10.1002/ajmg.1320250624 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas