Author:
Billard C.,Gillet P.,Signoret J.L.,Uicaut E.,Bertrand P.,Fardeau M.,Barthez-Carpentier M.A.,Santini J.J.
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference59 articles.
1. Absence of genetic heterogeneity in Duchenne Muscular Dystrophy shown by a linkage study using two cloned DNA sequences;O'Brien;J Med Genet,1983
2. Gene deletions in X-linked muscular dystrophy;Lindlof;Am J Hum Genet,1989
3. Localization and cloning of Xp 21 deletion breakpoints involved in muscular dystrophy;Monaco;Hum Genet,1987
4. Dystrophin: the protein product of the Duchenne muscular locus;Hoffman;Cell,1987
5. Recherches sur la paralysie musculaire pseudo-hypertrophique, ou paralysie myosclérosique;Duchenne;Arch Gén Méd,1968
Cited by
140 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献