Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal Xq - Wikidata - wikimedia - TriplyDB

Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal Xq

Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal Xq

http://www.wikidata.org/entity/Q35247517

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Isolation of a candidate gene for choroideremia Deletions in patients with classical choroideremia vary in size from 45 kb to several megabases Genetic mapping of X-linked albinism-deafness syndrome (ADFN) to Xq26.3-q27.I.Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21 Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders Derivation of clones from the choroideremia locus by preparative field inversion gel electrophoresis.A cytogenetic survey in Menkes disease: implications for the detection of chromosomal rearrangements in X linked disorders.Molecular and cytogenetic analysis of a familial microdeletion of Xq.Possible genetic heterogeneity in X linked hypohidrotic ectodermal dysplasia Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremia Multipoint linkage analysis in Menkes disease.High-resolution mapping of the X-linked hypohidrotic ectodermal dysplasia (EDA) locus.Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines.The human osteonectin gene (OSN) has TaqI and MspI polymorphisms An X-linked DraI RFLP recognized by cpX23 [DXS132]X-linked severe combined immunodeficiency: localization within the region Xq13.1-q21.1 by linkage and deletion analysis.A BstE II RFLP at the DXS153 locus.

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P2860

Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal Xq

http://www.wikidata.org/entity/Q35247517

description

1988 nî lūn-bûn

@nan

1988 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

1988 թվականի հոտեմբերին հրատարակված գիտական հոդված

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1988年の論文

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1988年論文

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1988年論文

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1988年論文

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1988年論文

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1988年論文

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1988年论文

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name

Molecular analysis of male-via ...... f 52 DNA probes on proximal Xq

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Molecular analysis of male-via ...... f 52 DNA probes on proximal Xq

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type

label

Molecular analysis of male-via ...... f 52 DNA probes on proximal Xq

@ast

Molecular analysis of male-via ...... f 52 DNA probes on proximal Xq

@en

prefLabel

Molecular analysis of male-via ...... f 52 DNA probes on proximal Xq

@ast

Molecular analysis of male-via ...... f 52 DNA probes on proximal Xq

@en

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American Journal of Human Genetics

P1476

Molecular analysis of male-via ...... f 52 DNA probes on proximal Xq

@en

P2093

Cremers FP

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Hofker MH

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Mikkelsen M

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Pearson PL

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Pfeiffer RA

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Ropers HH

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Tabor A

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Wieringa B

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van de Pol TJ

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P2860

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

Choroideremia, obesity, and congenital deafness

Cloning the gene for an inherited human disorder--chronic granulomatous disease--on the basis of its chromosomal location

Variable number of tandem repeat (VNTR) markers for human gene mapping.

Isolation of anonymous DNA sequences from within a submicroscopic X chromosomal deletion in a patient with choroideremia, deafness, and mental retardation

The 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.

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 chromosome

Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.

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1988-10-01T00:00:00Z

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3177387

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1715498

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