Haplotype and multipoint linkage analysis in Finnish choroideremia families (Q41278462)

29 September 2017

title

Haplotype and multipoint linkage analysis in Finnish choroideremia families (English)

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29 September 2017

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Albert de la Chapelle

8

object named as

A de la Chapelle

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29 September 2017

E M Sankila

1

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29 September 2017

T Lehner

2

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29 September 2017

A W Eriksson

3

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29 September 2017

H Forsius

4

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29 September 2017

J Kärnä

5

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29 September 2017

D Page

6

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29 September 2017

J Ott

7

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29 September 2017

publication date

1 December 1989

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29 September 2017

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29 September 2017

volume

84

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29 September 2017

issue

1

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29 September 2017

page(s)

66-70

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Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I

29 September 2017

cites work

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https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

Isolation of a cDNA clone for human X-linked 3-phosphoglycerate kinase by use of a mixture of synthetic oligodeoxyribonucleotides as a detection probe

1 reference

https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

Strategies for multilocus linkage analysis in humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

Extensive DNA sequence homologies between the human Y and the long arm of the X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

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

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https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

The genetic linkage map of the human X chromosome

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https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

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

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https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

A genetic linkage study of choroideremia

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https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

Choroideremia in interstitial deletion of the X chromosome

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https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

Homologies between X and Y chromosomes detected by DNA probes: localisation and evolution

1 reference

https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

Choroideremia; clinical and genetic aspects

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https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

Deletion of the DXS165 locus in patients with classical choroideremia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers

1 reference

https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

An anonymous single-copy X-chromosome RFLP for DXS72 from Xq13-Xq22 [HGM8 provisional no. DXS72].

1 reference

https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

A hereditary and clinical study of choroideremia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2575071

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/2575071

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

Genetic mapping of nine DNA markers in the q11----q22 region of the human X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2575071

12 December 2020

Report of the committee on human gene mapping by recombinant DNA techniques

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https://pubmed.ncbi.nlm.nih.gov/2575071

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/2575071

12 December 2020

Identifiers

DOI

10.1007/BF00210674

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Dimensions Publication ID

29 September 2017

1010867472

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