Regional localization on the human X of DNA segments cloned from flow sorted chromosomes.
about
Isolation of amplified DNA sequences from IMR-32 human neuroblastoma cells: facilitation by fluorescence-activated flow sorting of metaphase chromosomesIsolation and DNA sequence of a full-length cDNA clone for human X chromosome-encoded phosphoglycerate kinaseAbsence of linkage of Noonan syndrome to the neurofibromatosis type 1 locus.Multipoint mapping of adult onset polycystic kidney disease (PKD1) on chromosome 16.Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindred.Immunohistochemical studies show truncated dystrophins in the myotubes of three fetuses at risk for Duchenne muscular dystrophyLinkage studies and deletion screening in choroideremiaA genetic linkage study of a kindred with X-linked retinitis pigmentosa.Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.Linkage studies in Duchenne and Becker muscular dystrophies.Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.Linkage analysis in Usher syndrome type I (USH1) families from SpainDNA analysis in human diseaseMapping of the mouse X chromosome using random genomic probes and an interspecific mouse cross2004 William Allan Award address. Cloning of the DMD gene.Cosmid clones derived from both euchromatic and heterochromatic regions of the human Y chromosomeSorsby's fundus dystrophy in a family with a Ser-181-CVS mutation in the TIMP-3 gene: poor outcome after laser photocoagulation.Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphismLinkage of the Wiskott-Aldrich syndrome with polymorphic DNA sequences from the human X chromosome.Regional assignment of Y-linked DNA probes by deletion mapping and their homology with X-chromosome and autosomal sequencesDeletion mapping of the testis determining locus with DNA probes in 46,XX males and in 46,XY and 46,X,dic(Y) femalesLocalization of DNA sequences to a region within Xp11.21 between incontinentia pigmenti (IP1) X-chromosomal translocation breakpoints.Heterogeneity in X-linked recessive Charcot-Marie-Tooth neuropathy.Norrie disease gene is distinct from the monoamine oxidase genes.Absence of a single repeat from the coding region of the human involucrin gene leading to RFLPLinkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probesLocalization of the microsatellite probe DXS426 between DXS7 and DXS255 on Xp and linkage to X-linked retinitis pigmentosaThe X chromosome shows less genetic variation at restriction sites than the autosomes.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.DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21.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.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.A strategy to reveal high-frequency RFLPs along the human X chromosomeLocalization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus.Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutationAnalysis of three restriction fragment length polymorphisms in the human type II procollagen gene.Accurate and superaccurate gene mappingQuantitative analysis of sex-chromosome mosaicism with X-Y DNA probes.Identification and application of additional restriction fragment length polymorphisms at the human ornithine transcarbamylase locus
P2860
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P2860
Regional localization on the human X of DNA segments cloned from flow sorted chromosomes.
description
1982 nî lūn-bûn
@nan
1982 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1982 թվականի մարտին հրատարակված գիտական հոդված
@hy
1982年の論文
@ja
1982年論文
@yue
1982年論文
@zh-hant
1982年論文
@zh-hk
1982年論文
@zh-mo
1982年論文
@zh-tw
1982年论文
@wuu
name
Regional localization on the human X of DNA segments cloned from flow sorted chromosomes.
@ast
Regional localization on the human X of DNA segments cloned from flow sorted chromosomes.
@en
type
label
Regional localization on the human X of DNA segments cloned from flow sorted chromosomes.
@ast
Regional localization on the human X of DNA segments cloned from flow sorted chromosomes.
@en
prefLabel
Regional localization on the human X of DNA segments cloned from flow sorted chromosomes.
@ast
Regional localization on the human X of DNA segments cloned from flow sorted chromosomes.
@en
P2093
P2860
P356
P1476
Regional localization on the human X of DNA segments cloned from flow sorted chromosomes.
@en
P2093
L M Kunkel
M Eisenhard
U Tantravahi
P2860
P304
P356
10.1093/NAR/10.5.1557
P407
P577
1982-03-01T00:00:00Z