(Q33917686)

30 July 2017

title

DXS26 (HU16) is located in Xq21.1. (English)

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30 July 2017

author

Albert de la Chapelle

8

object named as

de la Chapelle A

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30 July 2017

Sankila EM

1

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30 July 2017

Bruns GA

2

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30 July 2017

Schwartz M

3

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30 July 2017

Nikoskelainen E

4

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30 July 2017

Niebuhr E

5

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30 July 2017

Hodgson SV

6

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30 July 2017

Wright AF

7

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30 July 2017

publication date

1 June 1990

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30 July 2017

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30 July 2017

volume

85

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30 July 2017

issue

1

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30 July 2017

page(s)

117-120

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Construction of a genetic linkage map in man using restriction fragment length polymorphisms

30 July 2017

cites work

1 reference

12 December 2020

Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms.

1 reference

12 December 2020

Isolation of DNA fragments from chromosome 13

1 reference

12 December 2020

Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremia

1 reference

12 December 2020

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

1 reference

12 December 2020

Complex glycerol kinase deficiency syndrome explained as X-chromosomal deletion

1 reference

12 December 2020

Choroideremia. A clinical and genetic study of 84 Finnish patients and 126 female carriers

1 reference

12 December 2020

Linkage studies with the gene for an X-linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2)

1 reference

12 December 2020

A non-syndromal form of X-linked mental retardation (XLMR) is linked to DXS14.

1 reference

12 December 2020

Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia

1 reference

12 December 2020

Strategies for studying heterogeneous genetic traits in humans by using a linkage map of restriction fragment length polymorphisms

1 reference

12 December 2020

X-linked cleft palate: the gene is localized between polymorphic DNA markers DXYS12 and DXS17

1 reference

12 December 2020

Linkage of an X-chromosome cleft palate gene

1 reference

12 December 2020

Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes.

1 reference

12 December 2020

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

1 reference

12 December 2020

Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletion.

1 reference

12 December 2020

Choroideremia in interstitial deletion of the X chromosome

1 reference

12 December 2020

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

12 December 2020

Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes

1 reference

12 December 2020

Interstitial deletion in the "critical region" of the long arm of the X chromosome in a mentally retarded boy and his normal mother.

1 reference

12 December 2020

Linkage analysis suggests at least two loci for X-linked non-specific mental retardation.

1 reference

12 December 2020

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

1 reference

12 December 2020

Regional assignment of the steroid sulfatase—X-linked ichthyosis locus: Implications for a noninactivated region on the short arm of human X chromosome

1 reference

12 December 2020

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

1 reference

12 December 2020

Choroideremia: close linkage to DXYS1 and DXYS12 demonstrated by segregation analysis and historical-genealogical evidence

1 reference

12 December 2020

Report of the committee on the genetic constitution of the X chromosome

1 reference

12 December 2020

A new syndrome with mental retardation, short stature and an Xq duplication.

1 reference

12 December 2020

Recognition and reanalysis of a cell line from a manifesting female with X linked hypohidrotic ectodermal dysplasia and an X; autosome balanced translocation

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00276335

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Dimensions Publication ID

30 July 2017

1023979733

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