Homozygous duplication at 10p11.21 in a boy clinical manifestations of Lin-Gettig syndrome (2010)
- Autores:
- Autores USP: OTTO, PAULO ALBERTO - IB ; ROSENBERG, CARLA - IB ; MORGANTE, ANGELA MARIA VIANNA - IB
- Unidade: IB
- Assunto: DOENÇAS GENÉTICAS
- Idioma: Inglês
- Imprenta:
- Local: Washingtom, DC
- Data de publicação: 2010
- Fonte:
- Título do periódico: Poster Abstracts
- Nome do evento: Annual Meeting of the American Society of Human Genetics
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ABNT
MAZZEU, Juliana Forte et al. Homozygous duplication at 10p11.21 in a boy clinical manifestations of Lin-Gettig syndrome. 2010, Anais.. Washingtom, DC: Instituto de Biociências, Universidade de São Paulo, 2010. . Acesso em: 28 mar. 2024. -
APA
Mazzeu, J. F., Zhang, F., Carvalho, C. M., Krepischi, A. C. V., Yatsenko, S., Pardono, E., et al. (2010). Homozygous duplication at 10p11.21 in a boy clinical manifestations of Lin-Gettig syndrome. In Poster Abstracts. Washingtom, DC: Instituto de Biociências, Universidade de São Paulo. -
NLM
Mazzeu JF, Zhang F, Carvalho CM, Krepischi ACV, Yatsenko S, Pardono E, Otto PA, Rosenberg C, Lupsski J, Vianna-Morgante AM. Homozygous duplication at 10p11.21 in a boy clinical manifestations of Lin-Gettig syndrome. Poster Abstracts. 2010 ;[citado 2024 mar. 28 ] -
Vancouver
Mazzeu JF, Zhang F, Carvalho CM, Krepischi ACV, Yatsenko S, Pardono E, Otto PA, Rosenberg C, Lupsski J, Vianna-Morgante AM. Homozygous duplication at 10p11.21 in a boy clinical manifestations of Lin-Gettig syndrome. Poster Abstracts. 2010 ;[citado 2024 mar. 28 ] - Identificação de um cromossomo marcador derivado do 8 por hibridação in situ fluorescente (fish)
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- Insight into the mechanisms and consequences of recurrent telomere capture associated with a sub-telomeric deletion
- Intragenic rearrangement of rbl gene in a (4 ; 13) translocation demonstrated by fish
- Caracterizacao de marcadores derivados de cromossomos sexuais atraves da hibridacao in situ por fluorescencia (fish)
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