A highly polymorphic locus in human DNA revealed by cosmid-derived probes
about
Isolation of a candidate gene for choroideremiaAn insertion deletion polymorphism associated with C-FESWaardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortiumDeletions in patients with classical choroideremia vary in size from 45 kb to several megabasesAn Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometryClinical, cytogenetic, and molecular characterization of seven patients with deletions of chromosome 22q13.3Exclusion of a schizophrenia susceptibility gene from the chromosome 5q11-q13 region: new data and a reanalysis of previous reports.Saturating the region of the polycystic kidney disease gene with NotI linking clones.Derivation of clones from the choroideremia locus by preparative field inversion gel electrophoresis.Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects.Linkage analysis in Marfan syndrome.Exclusion of autosomal dominant polycystic kidney disease type II (ADPKD2) from 160 cM of chromosome 1.Alu-primed polymerase chain reaction for regional assignment of 110 yeast artificial chromosome clones from the human X chromosome: identification of clones associated with a disease locus.Detection of de novo mutations and analysis of their origin in families with X linked hypohidrotic ectodermal dysplasia.Genetic linkage map of 46 DNA markers on human chromosome 16.Molecular dissection of a contiguous gene syndrome: frequent submicroscopic deletions, evolutionarily conserved sequences, and a hypomethylated "island" in the Miller-Dieker chromosome region.Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremiaGenetic linkage map of human chromosome 7 with 63 DNA markersA hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene.Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment.A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.Partial isodisomy for maternal chromosome 7 and short stature in an individual with a mutation at the COL1A2 locusPossible linkage of the estrogen receptor gene to breast cancer in a family with late-onset disease.Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization.Evidence against the reported linkage of the cutaneous melanoma-dysplastic nevus syndrome locus to chromosome Ip36.Linkage disequilibria between pairs of loci within a highly polymorphic region of chromosome 2Q.A deductive method of haplotype analysis in pedigreesIsolation and regional mapping of DNA sequences unique to human chromosome 21.A highly polymorphic locus in human DNA revealed by probes from cosmid 1-5 maps to chromosome 2q35----37Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to chromosome 19.Tightly linked flanking markers for the Lowe oculocerebrorenal syndrome, with application to carrier assessmentChromosomal localization of the human proenkephalin and prodynorphin genesGenetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B familiesIdentification of more than 500 RFLPs by screening random genomic clones.New polymorphisms at the DXS98 locus and confirmation of its location proximal to FRAXA by in situ hybridization.Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal XqIdentification and characterization of 23 RFLP loci by screening random cosmid genomic clones.Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndromeCRI-J177 (DYS152): a polymorphic Y chromosome locus.Molecular characterization of the marker chromosome associated with cat eye syndrome
P2860
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P2860
A highly polymorphic locus in human DNA revealed by cosmid-derived probes
description
1985 nî lūn-bûn
@nan
1985年の論文
@ja
1985年学术文章
@wuu
1985年学术文章
@zh-cn
1985年学术文章
@zh-hans
1985年学术文章
@zh-my
1985年学术文章
@zh-sg
1985年學術文章
@yue
1985年學術文章
@zh
1985年學術文章
@zh-hant
name
A highly polymorphic locus in human DNA revealed by cosmid-derived probes
@ast
A highly polymorphic locus in human DNA revealed by cosmid-derived probes
@en
type
label
A highly polymorphic locus in human DNA revealed by cosmid-derived probes
@ast
A highly polymorphic locus in human DNA revealed by cosmid-derived probes
@en
prefLabel
A highly polymorphic locus in human DNA revealed by cosmid-derived probes
@ast
A highly polymorphic locus in human DNA revealed by cosmid-derived probes
@en
P2860
P356
P1476
A highly polymorphic locus in human DNA revealed by cosmid-derived probes
@en
P2093
P2860
P304
P356
10.1073/PNAS.82.18.6206
P407
P577
1985-09-01T00:00:00Z