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...

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Asıl Yazarlar: 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.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: The American Society of Human Genetics 2000
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Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1287516/
https://ncbi.nlm.nih.gov/pubmed/10903929
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