Chromosome 1p36 deletion syndrome: a report on 4 cases

Chromosome 1p36 deletion syndrome (MIM #607872) was first described in 1997 by Shapira et al. This condition is compatible with a monosomy of the 1p36 band in the distal region of the short arm of chromosome 1 and is the most common terminal deletion in humans, with an estimated prevalence of approx...

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Detalhes bibliográficos
Autor principal: Candeias, Cristina (author)
Outros Autores: Mota Freitas, Manuela (author), Ribeiro, Joana (author), Oliveira, Fernanda Paula (author), Aguiar, Joaquim (author), Oliva Teles, Natália (author), Soares, Gabriela (author), Carrilho, Inês (author), Martins, Márcia (author), Correia, Hildeberto (author), Fonseca Silva, Maria da Luz (author)
Formato: conferenceObject
Idioma:eng
Publicado em: 2012
Assuntos:
Doenças Genéticas
Telomere
Deletion
1p36
Monosomy
Texto completo:http://hdl.handle.net/10400.18/803
País:Portugal
Oai:oai:repositorio.insa.pt:10400.18/803

Texto Completo

http://hdl.handle.net/10400.18/803

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