A gene for Meckel syndrome maps to chromosome 11q13.

Meckel syndrome (MKS) is a rare autosomal recessive lethal condition of unknown origin, characterized by (i) an occipital meningo-encephalocele with (ii) enlarged kidneys, with multicystic dysplasia and fibrotic changes in the portal area of the liver and with ductal proliferation, and (iii) postaxi...

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Detalhes bibliográficos
Main Authors: Roume, J, Genin, E, Cormier-Daire, V, Ma, H W, Mehaye, B, Attie, T, Razavi-Encha, F, Fallet-Bianco, C, Buenerd, A, Clerget-Darpoux, F, Munnich, A, Le Merrer, M
Formato: Artigo
Idioma:Inglês
Publicado em: 1998
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377494/
https://ncbi.nlm.nih.gov/pubmed/9758620
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