Exclusion mapping of chromosomal regions which cross hybridise to FSHD1A associated markers in FSHD1B

Facioscapulohumeral muscular dystrophy (FHSD) is a genetically heterogeneous, autosomal dominant primary disease of muscle. The predominant form of FSHD, which has been designated FSHD1A, has been localised to the 4q34 region of human chromosome 4. The disease locus (loci) for the remaining FSHD fam...

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Detaylı Bibliyografya
Asıl Yazarlar: Gilbert, J R, Speer, M C, Stajich, J, Clancy, R, Lewis, K, Qiu, H, Yamaoka, L, Kumar, A, Vance, J, Stewart, C, Rozear, M, Roses, A D, Pericak-Vance, M A
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1995
Konular:
Original Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051697/
https://ncbi.nlm.nih.gov/pubmed/8558552
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