Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference44 articles.
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3. Choroideremia, obesity, and congenital deafness;Ayazi;Amer. J. Ophthalmol,1981
4. Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal insufficiency associated with Xp21 interstitial deletion;Bartley;J. Pediatr,1986
5. The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK;Brunner;Hum. Genet,1988
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