Estimation of the male to female ratio of mutation rates from the segregation of X-chromosomal DNA haplotypes in Duchenne muscular dystrophy families
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00282088.pdf
Reference23 articles.
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2. Bucher K, Ioanescu V, Hanson J (1980) Frequency of new mutants among boys with Duchenne muscular dystrophy. Am J Med Genet 7:27?46
3. Camerino G, Grzeschik KH, Jaye M, de la Salle H, Tolstoshev P, Lecocq JP (1984) Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus). Proc Nat Acad Sci USA 81:498?502
4. Caskey CT, Nussbaum RL, Cohan LC, Pollack L (1980) Sporadic occurrence of Duchenne muscular dystrophy: evidence for new mutation. Clin Genet 18:329?341
5. Crow JF, Denniston C (1985) Mutation in human populations. Adv Hum Genet 14:59?123
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1. Determinants of the incidence of Duchenne muscular dystrophy;ANN TRANSL MED;2015
2. Mutation: Spontaneous Mutation in Germ Cells;Human Genetics;1997
3. Detection of de novo mutations and analysis of their origin in families with X linked hypohidrotic ectodermal dysplasia.;Journal of Medical Genetics;1994-04-01
4. 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.;Journal of Medical Genetics;1994-03-01
5. Molecular genetics and genetic counselling for Duchenne/Becker muscular dystrophy;Molecular and Cell Biology of Muscular Dystrophy;1993
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