Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids.
about
The major human erythroid DNA-binding protein (GF-1): primary sequence and localization of the gene to the X chromosomeMapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studiesFusion of the transcription factor TFE3 gene to a novel gene, PRCC, in t(X;1)(p11;q21)-positive papillary renal cell carcinomasNance-Horan syndrome: localization within the region Xp21.1-Xp22.3 by linkage analysisGenetic mapping of X-linked albinism-deafness syndrome (ADFN) to Xq26.3-q27.I.Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferaseConstruction, arraying, and high-density screening of large insert libraries of human chromosomes X and 21: their potential use as reference libraries.Molecular genetics of retinitis pigmentosaMolecular cloning and analysis of the fragile X region in manLinkage analysis of X linked retinitis pigmentosa in the Irish population.Clinical reinvestigation and linkage analysis in the family with Episkopi blindness (Norrie disease)Molecular genetics of the human X chromosome.A computer programme to calculate risk in X linked disorders using multiple marker loci.Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy familiesThe application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophy.Recognition and reanalysis of a cell line from a manifesting female with X linked hypohidrotic ectodermal dysplasia and an X; autosome balanced translocation.DNA analysis in human diseaseMapping the Lowe oculocerebrorenal syndrome to Xq24-q26 by use of restriction fragment length polymorphismsLinkage of the Wiskott-Aldrich syndrome with polymorphic DNA sequences from the human X chromosome.Histone modification patterns associated with the human X chromosomeEvolution of homologous sequences on the human X and Y chromosomes, outside of the meiotic pairing segment.Deletions within the pseudoautosomal region help map three new markers and indicate a possible role of this region in linear growth.A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: linkage mapping of the synapsin I/A-raf-1 genes.Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines.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.Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14.The use of multiple restriction fragment length polymorphisms in prenatal risk estimation. I. X-linked diseases.Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutationRegional mapping of six cloned DNA sequences on human chromosome 7.A DNA probe detecting multiple haplotypes of the human Y chromosome.Localization of the McLeod locus (XK) within Xp21 by deletion analysis.X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosisLocalization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis.Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal XqA long range restriction map of the pseudoautosomal region by partial digest PFGE analysis from the telomereIsolation of a conserved sequence deleted in Duchenne muscular dystrophy patients.Gene for OTC: characterisation and linkage to Duchenne muscular dystrophyHuman X chromosome markers and Duchenne muscular dystrophy.Cloned DNA probes regionally mapped to human chromosome 21 and their use in determining the origin of nondisjunction.Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion.
P2860
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P2860
Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids.
description
1984 nî lūn-bûn
@nan
1984 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1984 թվականի մարտին հրատարակված գիտական հոդված
@hy
1984年の論文
@ja
1984年論文
@yue
1984年論文
@zh-hant
1984年論文
@zh-hk
1984年論文
@zh-mo
1984年論文
@zh-tw
1984年论文
@wuu
name
Toward a complete linkage map ...... panel of somatic cell hybrids.
@ast
Toward a complete linkage map ...... panel of somatic cell hybrids.
@en
type
label
Toward a complete linkage map ...... panel of somatic cell hybrids.
@ast
Toward a complete linkage map ...... panel of somatic cell hybrids.
@en
prefLabel
Toward a complete linkage map ...... panel of somatic cell hybrids.
@ast
Toward a complete linkage map ...... panel of somatic cell hybrids.
@en
P2093
P2860
P1476
Toward a complete linkage map ...... panel of somatic cell hybrids
@en
P2093
Bhattacharya S
Pearson PL
Wieacker P
Williamson R
P2860
P304
P407
P577
1984-03-01T00:00:00Z