A Member of a Gene Family on Xp22.3, VCX-A, Is Deleted in Patients with X-Linked Nonspecific Mental Retardation

X-linked nonspecific mental retardation (MRX) has a frequency of 0.15% in the male population and is caused by defects in several different genes on the human X chromosome. Genotype-phenotype correlations in male patients with a partial nullisomy of the X chromosome have suggested that at least one...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Main Authors: Fukami, Maki, Kirsch, Stefan, Schiller, Simone, Richter, Alexandra, Benes, Vladimir, Franco, Brunella, Muroya, Koji, Rao, Ercole, Merker, Sabine, Niesler, Beate, Ballabio, Andrea, Ansorge, Wilhelm, Ogata, Tsutomu, Rappold, Gudrun A.
Format: Artigo
Sprog:Inglês
Udgivet: The American Society of Human Genetics 2000
Fag:
Articles
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1287516/
https://ncbi.nlm.nih.gov/pubmed/10903929
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker