Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia (Q68519094)

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25 September 2019

title

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

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25 September 2019

author name string

M Schwartz

1

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25 September 2019

H M Yang

2

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25 September 2019

E Niebuhr

3

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25 September 2019

T Rosenberg

4

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D C Page

5

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publication date

1 February 1988

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25 September 2019

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25 September 2019

volume

78

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25 September 2019

issue

2

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25 September 2019

page(s)

156-160

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Choroideremia: further evidence for assignment of the locus to Xq13-Xq21

25 September 2019

cites work

1 reference

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12 December 2020

Inheritance of choroideremia

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12 December 2020

Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene

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12 December 2020

A strategy to reveal high-frequency RFLPs along the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422216

12 December 2020

Choroideremia-locus maps between DXS3 and DXS11 on Xq

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422216

12 December 2020

An international system for human cytogenetic nomenclature--high-resolution banding (1981). ISCN (1981). Report of the Standing Committee on Human Cytogenetic Nomenclature

1 reference

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12 December 2020

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

1 reference

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12 December 2020

X-linked dominant Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal Xq.

1 reference

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12 December 2020

Mechanisms of chromosome banding and implications for chromosome structure

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12 December 2020

Linkage of an X-chromosome cleft palate gene

1 reference

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12 December 2020

Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphism

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12 December 2020

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

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12 December 2020

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

1 reference

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12 December 2020

Choroideremia in interstitial deletion of the X chromosome

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12 December 2020

Report of the Committee on the Genetic Constitution of the X and Y Chromosomes

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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

https://pubmed.ncbi.nlm.nih.gov/3422216

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422216

12 December 2020

Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion

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https://pubmed.ncbi.nlm.nih.gov/3422216

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

https://pubmed.ncbi.nlm.nih.gov/3422216

12 December 2020

A hereditary and clinical study of choroideremia

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422216

12 December 2020

Close linkage between X-linked ectodermal dysplasia and a cloned DNA sequence detecting a two allele restriction fragment length polymorphism in the region Xp11-q12

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422216

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422216

12 December 2020

Choroideremia is linked to the restriction fragment length polymorphism DXYS1 at XQ13-21.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422216

12 December 2020

Gene localisation of X-linked hypohidrotic ectodermal dysplasia (C-S-T syndrome)

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422216

12 December 2020

[Staining of human chromosomes with acridine orange after treatment with 5 bromodeoxyuridine]

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422216

12 December 2020

Choroideremia, congenital deafness and mental retardation in a family with an X chromosomal deletion.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422216

12 December 2020

Multipoint linkage analysis of loci in the proximal long arm of the human X chromosome: application to mapping the choroideremia locus.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422216

12 December 2020

Identifiers

DOI

10.1007/BF00278188

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25 September 2019

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