Isolation of anonymous DNA sequences from within a submicroscopic X chromosomal deletion in a patient with choroideremia, deafness, and mental retardation
about
Isolation of a candidate gene for choroideremiaDeletions in patients with classical choroideremia vary in size from 45 kb to several megabasesChoroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21An Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometryX-linked progressive mixed deafness: a new microdeletion that involves a more proximal region in Xq21.Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3)Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferaseSubtracted, unique-sequence, in situ hybridization: experimental and diagnostic applicationsDerivation of clones from the choroideremia locus by preparative field inversion gel electrophoresis.Linkage studies and deletion screening in choroideremiaMicrodeletion syndromes, balanced translocations, and gene mappingA maternally inherited 8.05 Mb Xq21 deletion associated with Choroideremia, deafness, and mental retardation syndrome in a male patient.Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremiaIsolation of YAC insert sequences by representational difference analysis.Genomic subtraction for cloning DNA corresponding to deletion mutations.The gene responsible for X-linked cleft palate (CPX) in a British Columbia native kindred is localized between PGK1 and DXYS1.Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss.Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal XqDetection of submicroscopic deletions in band 17p13 in patients with the Miller-Dieker syndrome.X-linked severe combined immunodeficiency: localization within the region Xq13.1-q21.1 by linkage and deletion analysis.Toward a cytogenetically based physical map of the wheat genome.A method for difference cloning: gene amplification following subtractive hybridization.Choroideremia: a review of general findings and pathogenesis.Localisation of two candidate genes for mental retardation using a YAC physical map of the Xq21.1-21.2 subbands.Deletion mapping of X-linked mixed deafness (DFN3) identifies a 265-525-kb region centromeric of DXS26.The pluses of subtraction.
P2860
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P2860
Isolation of anonymous DNA sequences from within a submicroscopic X chromosomal deletion in a patient with choroideremia, deafness, and mental retardation
description
1987 nî lūn-bûn
@nan
1987 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1987 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
name
Isolation of anonymous DNA seq ...... afness, and mental retardation
@ast
Isolation of anonymous DNA seq ...... afness, and mental retardation
@en
Isolation of anonymous DNA seq ...... afness, and mental retardation
@nl
type
label
Isolation of anonymous DNA seq ...... afness, and mental retardation
@ast
Isolation of anonymous DNA seq ...... afness, and mental retardation
@en
Isolation of anonymous DNA seq ...... afness, and mental retardation
@nl
prefLabel
Isolation of anonymous DNA seq ...... afness, and mental retardation
@ast
Isolation of anonymous DNA seq ...... afness, and mental retardation
@en
Isolation of anonymous DNA seq ...... afness, and mental retardation
@nl
P2093
P2860
P356
P1476
Isolation of anonymous DNA seq ...... afness, and mental retardation
@en
P2093
Ledbetter DH
Ledbetter SA
Nussbaum RL
P2860
P304
P356
10.1073/PNAS.84.18.6521
P407
P577
1987-09-01T00:00:00Z