Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21.
about
Studies of the locus for androgen receptor: localization on the human X chromosome and evidence for homology with the Tfm locus in the mouseMolecular analysis of a female Lesch-Nyhan patientThe William Allan Memorial Award. Presented to Patricia A. Jacobs, D.Sc., at the annual meeting of the American Society of Human Genetics, Dallas, October 28-31, 1981Molecular analysis of recombination in a family with Duchenne muscular dystrophy and a large pericentric X chromosome inversion.Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disordersGenetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosomeFurther evidence for Xp21 location of Duchenne muscular dystrophy (DMD) locus: X;9 translocation in a female with DMD.Cell surface abnormality in clones of skin fibroblasts from a carrier of Duchenne muscular dystrophy.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 dystrophyIsolating the gene for Duchenne muscular dystrophy.American Society of Human Genetics presidential address, October 18, 1990A practical metaphase marker of the inactive X chromosome.DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21.The William Allan Memorial Award address: Reverse genetics and beyondLocalization 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.Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.Accurate and superaccurate gene mappingA family with Huntington disease and reciprocal translocation 4;5.Partial trisomy 14 (q23 leads to qter) via segregation of a 14/X translocation.Tightly linked flanking markers for the Lowe oculocerebrorenal syndrome, with application to carrier assessmentSequence analysis of the breakpoint regions of an X;5 translocation in a female with Duchenne muscular dystrophy.An appraisal of the application of recombinant DNA techniques to chromosome defects
P2860
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P2860
Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21.
description
1981 nî lūn-bûn
@nan
1981 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1981 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1981年の論文
@ja
1981年論文
@yue
1981年論文
@zh-hant
1981年論文
@zh-hk
1981年論文
@zh-mo
1981年論文
@zh-tw
1981年论文
@wuu
name
Duchenne muscular dystrophy (D ...... that the DMD locus is at Xp21.
@ast
Duchenne muscular dystrophy (D ...... that the DMD locus is at Xp21.
@en
type
label
Duchenne muscular dystrophy (D ...... that the DMD locus is at Xp21.
@ast
Duchenne muscular dystrophy (D ...... that the DMD locus is at Xp21.
@en
prefLabel
Duchenne muscular dystrophy (D ...... that the DMD locus is at Xp21.
@ast
Duchenne muscular dystrophy (D ...... that the DMD locus is at Xp21.
@en
P2093
P2860
P1476
Duchenne muscular dystrophy (D ...... that the DMD locus is at Xp21.
@en
P2093
P2860
P304
P407
P577
1981-07-01T00:00:00Z