Analysis of linkage relationships of X-linked retinitis pigmentosa with the following Xp loci: L1.28, OTC, 754, XJ-1.1, pERT87, and C7 (Q68519079)

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25 September 2019

title

Analysis of linkage relationships of X-linked retinitis pigmentosa with the following Xp loci: L1.28, OTC, 754, XJ-1.1, pERT87, and C7 (English)

1 reference

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25 September 2019

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M J Denton

1

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25 September 2019

J D Chen

2

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25 September 2019

S Serravalle

3

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25 September 2019

P Colley

4

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25 September 2019

F B Halliday

5

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25 September 2019

J Donald

6

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25 September 2019

publication date

1 January 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

1

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25 September 2019

page(s)

60-64

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Mapping X-linked ophthalmic diseases: II. Linkage relationship of X-linked retinitis pigmentosa to X chromosomal short arm markers

25 September 2019

cites work

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422211

12 December 2020

X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422211

12 December 2020

Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422211

12 December 2020

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422211

12 December 2020

The electro-oculogram: analysis in a sample of normal human subjects and in selected retino-choroidal diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422211

12 December 2020

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422211

12 December 2020

X-linked recessive retinitis pigmentosa. Clinical characteristics of carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422211

12 December 2020

Linkage between the X-linked retinitis pigmentosa locus and the L1.28 locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422211

12 December 2020

Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422211

12 December 2020

Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422211

12 December 2020

Ophthalmoscopic Appearances of Peripheral Pigmentary Tapeto-retinal Dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422211

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422211

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/3422211

12 December 2020

Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422211

12 December 2020

Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3422211

12 December 2020

Identifiers

DOI

10.1007/BF00291236

1 reference

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25 September 2019

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