Carrier detection and gene analysis in a Duchenne muscular dystrophy family

Probe C7, pERT87-15, 754 which on the short arm of the X chromosome are used in the linkage analysis of a DMD family by the use of restriction fragment length porlymorphism (RFLP) and serum CPK, CPK-MB are detected. Three obligated carriers are determined and we also find a deletion to pERT87-15 in...

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Bibliographic Details
Published inZhonghua shen jing jing shen ke za zhi = Chinese journal of neurology and psychiatry Vol. 23; no. 4; p. 231
Main Author Lu, F M
Format Journal Article
LanguageChinese
Published China 01.08.1990
Subjects
Chromosome Deletion
Creatine Kinase - blood
DNA Probes
Genetic Linkage
Heterozygote
Humans
Isoenzymes
Male
Muscular Dystrophies - diagnosis
Muscular Dystrophies - genetics
Pedigree
Polymorphism, Restriction Fragment Length
X Chromosome
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Summary:Probe C7, pERT87-15, 754 which on the short arm of the X chromosome are used in the linkage analysis of a DMD family by the use of restriction fragment length porlymorphism (RFLP) and serum CPK, CPK-MB are detected. Three obligated carriers are determined and we also find a deletion to pERT87-15 in this family.
ISSN:0412-4057