Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen.

Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen.

Monosomy of the human chromosome 6p terminal region results in a variety of congenital malformations that include brain, craniofacial, and organogenesis abnormalities. To examine the genetic basis of these phenotypes, we have carried out an unbiased functional analysis of the syntenic region of the...

ver descrição completa

Detalhes bibliográficos
Principais autores: Bogani, D, Willoughby, C, Davies, J, Kaur, K, Mirza, G, Paudyal, A, Haines, H, McKeone, R, Cadman, M, Pieles, G, Schneider, J, Bhattacharya, S, Hardy, A, Nolan, P, Tripodis, N, Depew, M, Chandrasekara, R, Duncan, G, Sharpe, P, Greenfield, A, Denny, P, Brown, S, Ragoussis, J, Arkell, R
Formato: Journal article
Idioma:English
Publicado em: 2005

Registros relacionados

Registros relacionados