Author:
Hallwirth Pillay K.D.,Bill P.L.A.,Madurai S.,Mubaiwa L.,Rapiti P.
Subject
Neurology (clinical),Neurology
Reference11 articles.
1. Bakker E. Duchenne muscular dystrophy: Carrier detection and prenatal diagnosis by DNA analysis. New mutation and mosaicism. The Netherlands: PhD Thesis; 1989.
2. Complete cloning of Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals;Koenig;Cell,1987
3. Topography of the Duchenne muscular dystrophy (DMD) gene : FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications;Den Dunnen;Am J Hum Genet,1989
4. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction;Beggs;Hum Genet,1990
5. Duchenne and Becker muscular dystrophy prevalence in South Africa and molecular findings in 128 persons affected;Ballo;SAMJ S Afr Med J,1994
Cited by
11 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