Molecular deletion analysis in Duchenne muscular dystrophy.
about
Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disordersMild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome.Analysis of RFLPs and DNA deletions in the Chinese Duchenne muscular dystrophy geneLinkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophyPartial gene duplication in Duchenne and Becker muscular dystrophies.Partial gene duplication involving exon-Alu interchange results in lipoprotein lipase deficiency.Gene deletions in X-linked muscular dystrophy.Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene.
P2860
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P2860
Molecular deletion analysis in Duchenne muscular dystrophy.
description
1986 nî lūn-bûn
@nan
1986 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1986 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
name
Molecular deletion analysis in Duchenne muscular dystrophy.
@ast
Molecular deletion analysis in Duchenne muscular dystrophy.
@en
type
label
Molecular deletion analysis in Duchenne muscular dystrophy.
@ast
Molecular deletion analysis in Duchenne muscular dystrophy.
@en
prefLabel
Molecular deletion analysis in Duchenne muscular dystrophy.
@ast
Molecular deletion analysis in Duchenne muscular dystrophy.
@en
P2093
P2860
P356
P1476
Molecular deletion analysis in Duchenne muscular dystrophy
@en
P2093
P2860
P304
P356
10.1136/JMG.23.6.509
P407
P577
1986-12-01T00:00:00Z