Deletion mapping of the DXS986, DXS995, and DXS1002 loci defines their order within Xq21 - Wikidata - wikimedia - TriplyDB

Deletion mapping of the DXS986, DXS995, and DXS1002 loci defines their order within Xq21

Deletion mapping of the DXS986, DXS995, and DXS1002 loci defines their order within Xq21

http://www.wikidata.org/entity/Q33673926

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Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal families.Trisomy X in a female member of a family with X linked severe combined immunodeficiency: implications for carrier diagnosis.

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P2860

Deletion mapping of the DXS986, DXS995, and DXS1002 loci defines their order within Xq21

http://www.wikidata.org/entity/Q33673926

description

1994 nî lūn-bûn

@nan

1994 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

1994 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

1994年の論文

@ja

1994年論文

@yue

1994年論文

@zh-hant

1994年論文

@zh-hk

1994年論文

@zh-mo

1994年論文

@zh-tw

1994年论文

@wuu

name

Deletion mapping of the DXS986, DXS995, and DXS1002 loci defines their order within Xq21

@ast

Deletion mapping of the DXS986, DXS995, and DXS1002 loci defines their order within Xq21

@en

type

label

Deletion mapping of the DXS986, DXS995, and DXS1002 loci defines their order within Xq21

@ast

Deletion mapping of the DXS986, DXS995, and DXS1002 loci defines their order within Xq21

@en

prefLabel

Deletion mapping of the DXS986, DXS995, and DXS1002 loci defines their order within Xq21

@ast

Deletion mapping of the DXS986, DXS995, and DXS1002 loci defines their order within Xq21

@en

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Journal of Medical Genetics

P1476

Deletion mapping of the DXS986, DXS995, and DXS1002 loci defines their order within Xq21

@en

P2093

Clark PA

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Fontes M

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Kinnon C

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Lester T

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Villard L

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P2860

Fine mapping and cloning of the breakpoint associated with Menkes syndrome in a female patient.

Characterization of a 1.0 Mb YAC contig spanning two chromosome breakpoints related to Menkes disease.

A second-generation linkage map of the human genome.

X-linked severe combined immunodeficiency: localization within the region Xq13.1-q21.1 by linkage and deletion analysis.

The interleukin-2 receptor gamma chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1.

Dinucleotide repeat polymorphism at the DXS441 locus.

Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome.

A simple, efficient method for the separate isolation of RNA and DNA from the same cells.

X-linked mental retardation: in pursuit of a gene map.

Physical fine mapping of genes underlying X-linked deafness and non fra (X)-X-linked mental retardation at Xq21.

P304

344-345

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scholarly article

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10.1136/JMG.31.4.344

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4

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31

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1994-04-01T00:00:00Z

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15127214

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8071966

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1049814

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