Home
LiteratureArticle Details
PMID: 5387424
Published · ppublish
English
Journal Article
Carrier detection in X-linked muscular dystrophy.
Journal de genetique humaine
·Vol. 17
·No. 3
·1969-10-00
·Pages 497-510
Abstract
暂无摘要
MeSH Terms
Biopsy
Chromosome Aberrations
Chromosome Disorders
Creatine Kinase/blood
Crossing Over, Genetic
Diagnosis, Differential
Electromyography
Female
Genes, Recessive
Heterozygote
Humans
Male
Muscular Dystrophies/diagnosis,enzymology,genetics
Sex Chromosome Aberrations
Sex Factors
Chemicals
Creatine Kinase
Article Info
Journal
Journal de genetique humaine
Abbr.
J Genet Hum
ISSN
0021-7743
Published
1969-10-00
Pages
497-510
Language
English
Region
Switzerland
NLM ID
2983308R
Subset
IM
External Links
PubMed source
Analysis Services
Contact
No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong
Qilu Normal University · Genelibs Bioinformatics Lab
750 Shunhua Rd, Jinan
2F, Bldg F, University Science Park
Tel: 0531-88819269
WeChat Official Account
Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.
Business Email
E-mail: product@genelibs.com
Copyright © 2026.Genelibs Jinan Honghui Biotechnology Co., Ltd. 鲁ICP备20007159号-2
