(Q28282607)

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Genetic linkage between X-linked retinitis pigmentosa and DNA probe DXS7 (L1.28): further linkage data, heterogeneity testing, and risk estimation

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scholarly article

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Genetic linkage between X-linked retinitis pigmentosa and DNA probe DXS7 (L1.28): further linkage data, heterogeneity testing, and risk estimation (English)

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retinitis pigmentosa

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based on heuristic

inferred from title

author name string

J F Clayton

1

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A F Wright

2

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M Jay

3

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C M McKeown

4

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M Dempster

5

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B S Jay

6

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A C Bird

7

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S S Bhattacharya

8

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publication date

October 1986

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language of work or name

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74

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2

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168-71

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2876947

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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/2876947

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genetic linkage study of a kindred with X-linked retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/2876947

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the Committee on Methods of Linkage Analysis and Reporting

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https://pubmed.ncbi.nlm.nih.gov/2876947

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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/2876947

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis and family classification under heterogeneity

1 reference

https://pubmed.ncbi.nlm.nih.gov/2876947

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2876947

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An analysis procedure illustrated on a triple linkage of use for prenatal diagnosis of myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2876947

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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/2876947

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TESTING FOR HETEROGENEITY OF RECOMBINATION FRACTION VALUES IN HUMAN GENETICS

1 reference

https://pubmed.ncbi.nlm.nih.gov/2876947

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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/2876947

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2876947

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked retinitis pigmentosa

1 reference

https://pubmed.ncbi.nlm.nih.gov/2876947

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00282083

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