On the origin of deletions and point mutations in Duchenne muscular dystrophy: most deletions arise in oogenesis and most point mutations result from events in spermatogenesis.-Reference-Cited by-同舟云学术

On the origin of deletions and point mutations in Duchenne muscular dystrophy: most deletions arise in oogenesis and most point mutations result from events in spermatogenesis.

Published:1994-03-01 Issue:3 Volume:31 Page:183-186
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Grimm T,Meng G,Liechti-Gallati S,Bettecken T,Muller C R,Muller B

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference12 articles.

1. Estimation of the male to female ratio of mutation rates from the segregation of X chromosomal DNA haplotypes in Duchenne muscular dystrophy families;Muller, C.R.; Grimm, T.;Hum Genet,1986

2. Estimation of the male and female mutation rates in Duchenne muscular dystrophy (DMD);Muller, B.; Dechant, C.; Meng, G.;Hum Genet,1992

3. Different mosaicism frequencies for proximal and distal Duchenne muscular dystrophy (DMD) mutations indicate difference in etiology and recurrence risk;Passos-Bueno, M.R.; Bakker, E.; Kneppers, A.L.J.;Am J Hum Genet,1992

4. te Meerman GJ, ten Kate LP. Birth and population prevalence of Duchenne muscular dystrophy in the Netherlands;van Essen AJ; HFM, Busch;Hum Genet,1992

5. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals;Koenig, M.; Hoffman, E.P.; Bertelson, C.J.; Monaco, A.P.; Feener, C.; Kunkel, L.M.;Cell,1987

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