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8 in total

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

Authors: U Friedrich; M Warburg; P Wieacker; T F Wienker; A Gal; H H Ropers
Journal: Hum Genet Date: 1985 Impact factor: 4.132

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

Authors: M J Denton; J D Chen; S Serravalle; P Colley; F B Halliday; J Donald
Journal: Hum Genet Date: 1988-01 Impact factor: 4.132

3. 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.

Authors: A F Wright; S S Bhattacharya; J F Clayton; M Dempster; P Tippett; C M McKeown; M Jay; B Jay; A C Bird
Journal: Am J Hum Genet Date: 1987-10 Impact factor: 11.025

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

Authors: J Ott
Journal: Am J Hum Genet Date: 1974-09 Impact factor: 11.025

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

Authors: R L Nussbaum; R A Lewis; J G Lesko; R Ferrell
Journal: Hum Genet Date: 1985 Impact factor: 4.132

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

Authors: J F Clayton; A F Wright; M Jay; C M McKeown; M Dempster; B S Jay; A C Bird; S S Bhattacharya
Journal: Hum Genet Date: 1986-10 Impact factor: 4.132

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

Authors: S S Bhattacharya; A F Wright; J F Clayton; W H Price; C I Phillips; C M McKeown; M Jay; A C Bird; P L Pearson; E M Southern
Journal: Nature Date: 1984 May 17-23 Impact factor: 49.962

8. Prevalence of retinitis pigmentosa in Maine.

Authors: C H Bunker; E L Berson; W C Bromley; R P Hayes; T H Roderick
Journal: Am J Ophthalmol Date: 1984-03 Impact factor: 5.258

8 in total

1 in total

1. Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremia.

Authors: F P Cremers; D J van de Pol; B Wieringa; F S Collins; E M Sankila; V M Siu; W F Flintoff; F Brunsmann; L A Blonden; H H Ropers
Journal: Proc Natl Acad Sci U S A Date: 1989-10 Impact factor: 11.205

1 in total