Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus.
about
Analysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinismNance-Horan syndrome: localization within the region Xp21.1-Xp22.3 by linkage analysisAssignment of human genes for phosphorylase kinase subunits alpha (PHKA) to Xq12-q13 and beta (PHKB) to 16q12-q13Chromosomal localization of the gene for the human trifunctional enzyme, methylenetetrahydrofolate dehydrogenase-methenyltetrahydrofolate cyclohydrolase-formyltetrahydrofolate synthetaseLocalisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy familiesLinkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophyThe application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophy.Bridging markers defining the map position of X linked hypophosphataemic rickets.X linked spondyloepiphyseal dysplasia: a clinical, radiological, and molecular study of a large kindred.Genetic and cytogenetic localisation of the homeo box containing genes on mouse chromosome 6 and human chromosome 7.Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions.Common sequence motifs at the rearrangement sites of a constitutional X/autosome translocation and associated deletion.Translocation of the nucleolus organizer region to the human X chromosome.Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardation.Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.Localization of the McLeod locus (XK) within Xp21 by deletion analysis.Deletion mapping and X inactivation analysis of a non-specific mental retardation gene at Xp21.3-Xp22.11DNA linkage analysis of X chromosome-linked chronic granulomatous diseaseGenes for synapsin I, a neuronal phosphoprotein, map to conserved regions of human and murine X chromosomes.Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion.Upregulation of the creatine synthetic pathway in skeletal muscles of mature mdx mice.
P2860
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P2860
Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus.
description
1985 nî lūn-bûn
@nan
1985 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1985 թվականի մարտին հրատարակված գիտական հոդված
@hy
1985年の論文
@ja
1985年論文
@yue
1985年論文
@zh-hant
1985年論文
@zh-hk
1985年論文
@zh-mo
1985年論文
@zh-tw
1985年论文
@wuu
name
Localization of DNA sequences ...... enne muscular dystrophy locus.
@ast
Localization of DNA sequences ...... enne muscular dystrophy locus.
@en
type
label
Localization of DNA sequences ...... enne muscular dystrophy locus.
@ast
Localization of DNA sequences ...... enne muscular dystrophy locus.
@en
prefLabel
Localization of DNA sequences ...... enne muscular dystrophy locus.
@ast
Localization of DNA sequences ...... enne muscular dystrophy locus.
@en
P2093
P2860
P1476
Localization of DNA sequences ...... henne muscular dystrophy locus
@en
P2093
B de Martinville
J L Mandel
L M Kunkel
P2860
P304
P407
P577
1985-03-01T00:00:00Z