Evidence of neuronal migration disorders in knobloch syndrome: clinical and molecular analysis of two novel families (2003)
- Authors:
- USP affiliated authors: ROSEMBERG, SERGIO - FM ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB
- Unidades: FM; IB
- DOI: 10.1002/ajmg.a.20070
- Subjects: OFTALMOPATIAS (IMUNOLOGIA); OFTALMOPATIAS (GENÉTICA); ANTICORPOS; BIOLOGIA MOLECULAR
- Language: Inglês
- Imprenta:
- Publisher place: Reino Unido
- Date published: 2003
- Source:
- Título do periódico: American Journal of Medical Genetics
- ISSN: 0148-7299
- Volume/Número/Paginação/Ano: v. 119 A, n. 1, p. 15-19, 2003
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
KLIEMANN, Susana et al. Evidence of neuronal migration disorders in knobloch syndrome: clinical and molecular analysis of two novel families. American Journal of Medical Genetics, v. 119 A, n. 1, p. 15-19, 2003Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.20070. Acesso em: 19 abr. 2024. -
APA
Kliemann, S., Waetge, R. T. L., Suzuki, O. T., Passos-Bueno, M. R., & Rosemberg, S. (2003). Evidence of neuronal migration disorders in knobloch syndrome: clinical and molecular analysis of two novel families. American Journal of Medical Genetics, 119 A( 1), 15-19. doi:10.1002/ajmg.a.20070 -
NLM
Kliemann S, Waetge RTL, Suzuki OT, Passos-Bueno MR, Rosemberg S. Evidence of neuronal migration disorders in knobloch syndrome: clinical and molecular analysis of two novel families [Internet]. American Journal of Medical Genetics. 2003 ; 119 A( 1): 15-19.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.20070 -
Vancouver
Kliemann S, Waetge RTL, Suzuki OT, Passos-Bueno MR, Rosemberg S. Evidence of neuronal migration disorders in knobloch syndrome: clinical and molecular analysis of two novel families [Internet]. American Journal of Medical Genetics. 2003 ; 119 A( 1): 15-19.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.20070 - Molecular analysis of collagen XVIII reveals novel mutations, presence of a third isoform, and possible genetic heterogeneity in Knobloch syndrome
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Informações sobre o DOI: 10.1002/ajmg.a.20070 (Fonte: oaDOI API)
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