Insertional translocation of 15q25-q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridia (2012)
- Authors:
- Simioni, Milena - Universidade Estadual de Campinas (UNICAMP)
- Vieira, Tarsis Paiva - Universidade Estadual de Campinas (UNICAMP)
- Sgardioli, Ilária Cristina - Universidade Estadual de Campinas (UNICAMP)
- Freitas, Érika Lopes
- Rosenberg, Carla
- Maurer-Morelli, Cláudia Vianna - Universidade Estadual de Campinas (UNICAMP)
- Lopes-Cendes, Iscia - Universidade Estadual de Campinas (UNICAMP)
- Fett-Conte, Agnes Cristina
- Lopes, Vera Lúcia Gil da Silva - Universidade Estadual de Campinas (UNICAMP)
- Autor USP: ROSENBERG, CARLA - IB
- Unidade: IB
- DOI: 10.1002/ajmg.a.35603
- Subjects: HIBRIDIZAÇÃO; GENÔMICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American Journal of Medical Genetics. Part A
- ISSN: 1552-4825
- Volume/Número/Paginação/Ano: v. 158, n. 11, p. 2905-2910, 2012
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
SIMIONI, Milena et al. Insertional translocation of 15q25-q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridia. American Journal of Medical Genetics. Part A, v. 158, n. 11, p. 2905-2910, 2012Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.35603. Acesso em: 23 abr. 2024. -
APA
Simioni, M., Vieira, T. P., Sgardioli, I. C., Freitas, É. L., Rosenberg, C., Maurer-Morelli, C. V., et al. (2012). Insertional translocation of 15q25-q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridia. American Journal of Medical Genetics. Part A, 158( 11), 2905-2910. doi:10.1002/ajmg.a.35603 -
NLM
Simioni M, Vieira TP, Sgardioli IC, Freitas ÉL, Rosenberg C, Maurer-Morelli CV, Lopes-Cendes I, Fett-Conte AC, Lopes VLG da S. Insertional translocation of 15q25-q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridia [Internet]. American Journal of Medical Genetics. Part A. 2012 ; 158( 11): 2905-2910.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1002/ajmg.a.35603 -
Vancouver
Simioni M, Vieira TP, Sgardioli IC, Freitas ÉL, Rosenberg C, Maurer-Morelli CV, Lopes-Cendes I, Fett-Conte AC, Lopes VLG da S. Insertional translocation of 15q25-q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridia [Internet]. American Journal of Medical Genetics. Part A. 2012 ; 158( 11): 2905-2910.[citado 2024 abr. 23 ] Available from: https://doi.org/10.1002/ajmg.a.35603 - Number of rare germline CNVs and TP53 mutation types
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Informações sobre o DOI: 10.1002/ajmg.a.35603 (Fonte: oaDOI API)
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