Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm
about
Active and inactive genes localize preferentially in the periphery of chromosome territoriesDeletions of fetal and adult muscle cDNA in Duchenne and Becker muscular dystrophy patients.Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disordersAnalysis of RFLPs and DNA deletions in the Chinese Duchenne muscular dystrophy geneScreening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locusFurther evidence for Xp21 location of Duchenne muscular dystrophy (DMD) locus: X;9 translocation in a female with DMD.Molecular genetics of the human X chromosome.Duchenne muscular dystrophy in a female with a translocation involving Xp21.Muscular dystrophy in girls with X;autosome translocations.Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophyMolecular deletion analysis in Duchenne muscular dystrophy.Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophyCarrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.X inactivation analysis in a female with hypomelanosis of Ito associated with a balanced X;17 translocation: evidence for functional disomy of Xp.Isolating the gene for Duchenne muscular dystrophy.Neurogenetics: advancing the "next-generation" of brain research.A practical metaphase marker of the inactive X chromosome.Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus.Mapping of X-linked Becker muscular dystrophy through crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybrids.A family with Huntington disease and reciprocal translocation 4;5.Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21.Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosomeHuman X chromosome markers and Duchenne muscular dystrophy.Phenotypic contrasts of Duchenne Muscular Dystrophy in women: Two case reports.Innate immunity and the new forward genetics.An appraisal of the application of recombinant DNA techniques to chromosome defectsThe female carrier of Duchenne muscular dystrophy.
P2860
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P2860
Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm
description
1979 nî lūn-bûn
@nan
1979 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1979 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1979年の論文
@ja
1979年論文
@yue
1979年論文
@zh-hant
1979年論文
@zh-hk
1979年論文
@zh-mo
1979年論文
@zh-tw
1979年论文
@wuu
name
Muscular dystrophy in an X; 1 ...... s is on X chromosome short arm
@ast
Muscular dystrophy in an X; 1 ...... s is on X chromosome short arm
@en
Muscular dystrophy in an X; 1 ...... is on X chromosome short arm.
@nl
type
label
Muscular dystrophy in an X; 1 ...... s is on X chromosome short arm
@ast
Muscular dystrophy in an X; 1 ...... s is on X chromosome short arm
@en
Muscular dystrophy in an X; 1 ...... is on X chromosome short arm.
@nl
prefLabel
Muscular dystrophy in an X; 1 ...... s is on X chromosome short arm
@ast
Muscular dystrophy in an X; 1 ...... s is on X chromosome short arm
@en
Muscular dystrophy in an X; 1 ...... is on X chromosome short arm.
@nl
P2093
P2860
P1476
Muscular dystrophy in an X; 1 ...... s is on X chromosome short arm
@en
P2093
P2860
P304
P407
P577
1979-10-01T00:00:00Z