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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 1995
Pynciau:
Original Articles
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051697/
https://ncbi.nlm.nih.gov/pubmed/8558552
Tagiau: Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!

Eitemau Tebyg