Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation.

A somatic cell hybrid has been constructed and characterized using fibroblasts from a phenotypically normal woman who possesses an X chromosome with an interstitial deletion of the short arm. High-resolution banding indicates that the deleted segment is either Xp22.13-p11.4 or Xp22.11-p11.23. Southe...

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Detaylı Bibliyografya
Asıl Yazarlar: Ingle, C, Williamson, R, de la Chapelle, A, Herva, R R, Haapala, K, Bates, G, Willard, H F, Pearson, P, Davies, K E
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1985
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1684591/
https://ncbi.nlm.nih.gov/pubmed/2988331
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