Heterozygosity probabilities for normal relatives of isolated cases affected by incompletely penetrant dominant conditions and the calculation of recurrence risks for their offspring: I. autosomal dominant genes (2000)
- Autores:
- Autor USP: OTTO, PAULO ALBERTO - IB
- Unidade: IB
- DOI: 10.1002/1096-8628(20001106)95:1%3C43::aid-ajmg9%3E3.3.co;2-x
- Assunto: DOENÇAS GENÉTICAS
- Idioma: Inglês
- Imprenta:
- Fonte:
- Título do periódico: American Journal of Medical Genetics
- ISSN: 0148-7299
- Volume/Número/Paginação/Ano: v. 95, n. 43-48, 2000
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
OTTO, Paulo A e MAESTRELLI, Sylvia Regina Pedrosa. Heterozygosity probabilities for normal relatives of isolated cases affected by incompletely penetrant dominant conditions and the calculation of recurrence risks for their offspring: I. autosomal dominant genes. American Journal of Medical Genetics, v. 95, n. 43-48, 2000Tradução . . Disponível em: https://doi.org/10.1002/1096-8628(20001106)95:1%3C43::aid-ajmg9%3E3.3.co;2-x. Acesso em: 18 abr. 2024. -
APA
Otto, P. A., & Maestrelli, S. R. P. (2000). Heterozygosity probabilities for normal relatives of isolated cases affected by incompletely penetrant dominant conditions and the calculation of recurrence risks for their offspring: I. autosomal dominant genes. American Journal of Medical Genetics, 95( 43-48). doi:10.1002/1096-8628(20001106)95:1%3C43::aid-ajmg9%3E3.3.co;2-x -
NLM
Otto PA, Maestrelli SRP. Heterozygosity probabilities for normal relatives of isolated cases affected by incompletely penetrant dominant conditions and the calculation of recurrence risks for their offspring: I. autosomal dominant genes [Internet]. American Journal of Medical Genetics. 2000 ; 95( 43-48):[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/1096-8628(20001106)95:1%3C43::aid-ajmg9%3E3.3.co;2-x -
Vancouver
Otto PA, Maestrelli SRP. Heterozygosity probabilities for normal relatives of isolated cases affected by incompletely penetrant dominant conditions and the calculation of recurrence risks for their offspring: I. autosomal dominant genes [Internet]. American Journal of Medical Genetics. 2000 ; 95( 43-48):[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/1096-8628(20001106)95:1%3C43::aid-ajmg9%3E3.3.co;2-x - Unusual type of brachydactyly associated with short stature and facial anomalies: a new syndrome? [Brief clinical report]
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Informações sobre o DOI: 10.1002/1096-8628(20001106)95:1%3C43::aid-ajmg9%3E3.3.co;2-x (Fonte: oaDOI API)
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