Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests (Q24559869)

2

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J D Chen

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M J Denton

4

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J Donald

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C Dubay

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G J Farrar

7

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G A Fishman

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D Frey

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A Gal

Proceedings of the National Academy of Sciences of the United States of America

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language of work or name

English

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publication date

January 1990

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published in

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volume

87

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page(s)

701-4

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issue

2

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cites work

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

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

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The population genetics of Duchenne: natural and artificial selection in Duchenne muscular dystrophy

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Linkage analysis of X linked retinitis pigmentosa in the Irish population.

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Efficient computations in multilocus linkage analysis

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Duchenne muscular dystrophy with adrenal insufficiency and glycerol kinase deficiency: high resolution cytogenetic analysis with molecular, biochemical, and clinical studies

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Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis

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Risk calculations under heterogeneity

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Two different genes for X-linked retinitis pigmentosa

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

30 May 2018

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12 December 2020

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

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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

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12 December 2020

A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosome

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12 December 2020