Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? (1993)
- Authors:
- USP affiliated authors: ROSEMBERG, SERGIO - FM ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ZATZ, MAYANA - IB
- Unidades: FM; IB
- DOI: 10.1002/ajmg.1320460214
- Assunto: GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título: American Journal of Medical Genetics
- Volume/Número/Paginação/Ano: v.46, n.2 , p.172-5, 1993
- Status:
- Artigo possui versão em acesso aberto em repositório (Green Open Access)
- Versão do Documento:
- Versão publicada (Published version)
- Acessar versão aberta:
-
ABNT
PASSOS-BUENO, Maria Rita et al. Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation?. American Journal of Medical Genetics, v. 46, n. 2 , p. 172-5, 1993Tradução . . Disponível em: https://doi.org/10.1002/ajmg.1320460214. Acesso em: 07 maio 2026. -
APA
Passos-Bueno, M. R., Byth, B. C., Rosemberg, S., Takata, R. I., Bakker, E., Beggs, A. H., et al. (1993). Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? American Journal of Medical Genetics, 46( 2 ), 172-5. doi:10.1002/ajmg.1320460214 -
NLM
Passos-Bueno MR, Byth BC, Rosemberg S, Takata RI, Bakker E, Beggs AH, Pavanello RCM, Vainzof M, Davies KE, Zatz M. Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? [Internet]. American Journal of Medical Genetics. 1993 ;46( 2 ): 172-5.[citado 2026 maio 07 ] Available from: https://doi.org/10.1002/ajmg.1320460214 -
Vancouver
Passos-Bueno MR, Byth BC, Rosemberg S, Takata RI, Bakker E, Beggs AH, Pavanello RCM, Vainzof M, Davies KE, Zatz M. Severe nonspecific x-linked mental retardation caused by a proximally xp located gene: intragenic heterogeneity or a new form of x-linked mental retardation? [Internet]. American Journal of Medical Genetics. 1993 ;46( 2 ): 172-5.[citado 2026 maio 07 ] Available from: https://doi.org/10.1002/ajmg.1320460214 - Fine mapping and clinical reevaluation of a Brazilian pedigree with a severe form of X-linked mental retardation associated with other neurological dysfunction
- Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome
- Evidence of neuronal migration disorders in knobloch syndrome: clinical and molecular analysis of two novel families
- Human prion protein gene mutation at codon 183 associated with an atypical form of prion disease
- Friedreich's ataxia: clinical and molecular study of 25 brazilian cases
- Clinical and molecular aspects of 25 Brazilian friedreich's patients
- Clinical and molecular aspects of 25 brazilian Friedreich's patients
- Comparacao de 5 locos dinamicos em individuos caucasoides, negroides e orientais
- Molecular biology enhancing our understanding and improving the prevention of hereditary myopathies in the brazilian population
- Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 brazilian families
Informações sobre a disponibilidade de versões do artigo em acesso aberto coletadas automaticamente via oaDOI API (Unpaywall).
Por se tratar de integração com serviço externo, podem existir diferentes versões do trabalho (como preprints ou postprints), que podem diferir da versão publicada.
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
