Muscular dystrophy in girls with X;autosome translocations.

Twenty known cases of X;autosome translocations with breakpoints at Xp21 associated with Duchenne or Becker muscular dystrophy in girls are reviewed. The variable severity described for different persons may reflect differences in X inactivation or in the nature of the genomic target disrupted. High...

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Detaylı Bibliyografya
Asıl Yazarlar: Boyd, Y, Buckle, V, Holt, S, Munro, E, Hunter, D, Craig, I
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1986
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1049827/
https://ncbi.nlm.nih.gov/pubmed/3806636
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