Partial gene duplication in Duchenne and Becker muscular dystrophies.

Author:

Hu X Y,Burghes A H,Ray P N,Thompson M W,Murphy E G,Worton R G

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference28 articles.

1. Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy;Murray, J.M.; Davies, K.E.; Harper, P.S.; Meredith, L.; Mueller, C.R.; Williamson, R.;Nature,1982

2. Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophy;Brown, C.S.; Thomas, N.S.T.; Sarfarazi, M.;Hum Genet,1985

3. Muscular dystrophy in girls with X; autosome translocations;Boyd, Y.; Buckle, V.; Holt, S.; Munro, E.; Hunter, D.; Craig, I.;J Med Genet,1986

4. Minor Xp2l chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retiniiis pigmentosa, and McLeod syndrome;Francke, U.; Ochs, H.D.; de Martinville, B.;Am J Hum Genet,1985

5. Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal insufficiency associated with Xp2l interstitial deletion;Bartley, J.A.; Patil, S.; Davenport, S.; Goldstein, D.; Pickens, J.;J Pediatr,1986

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