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24. Linkage heterogeneity between X-linked retinitis pigmentosa and a map of 10 RFLP loci. Chen JD; Halliday F; Keith G; Sheffield L; Dickinson P; Gray R; Constable I; Denton M Am J Hum Genet; 1989 Sep; 45(3):401-11. PubMed ID: 2570529 [TBL] [Abstract][Full Text] [Related]
25. Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis. Musarella MA; Burghes A; Anson-Cartwright L; Mahtani MM; Argonza R; Tsui LC; Worton R Am J Hum Genet; 1988 Oct; 43(4):484-94. PubMed ID: 2902787 [TBL] [Abstract][Full Text] [Related]
26. Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28. Bhattacharya SS; Wright AF; Clayton JF; Price WH; Phillips CI; McKeown CM; Jay M; Bird AC; Pearson PL; Southern EM Nature; 1984 May 17-23; 309(5965):253-5. PubMed ID: 6325945 [TBL] [Abstract][Full Text] [Related]
27. A family with RP3 type of X-linked retinitis pigmentosa: an association with ciliary abnormalities. van Dorp DB; Wright AF; Carothers AD; Bleeker-Wagemakers EM Hum Genet; 1992 Jan; 88(3):331-4. PubMed ID: 1733835 [TBL] [Abstract][Full Text] [Related]
28. Carrier detection in X-linked retinitis pigmentosa. Gurvitz A; Leigh DA; Halliday F; Lai LY; McDonald BL Aust N Z J Ophthalmol; 1994 May; 22(2):111-3. PubMed ID: 7917263 [TBL] [Abstract][Full Text] [Related]
29. Mapping X-linked ophthalmic diseases: II. Linkage relationship of X-linked retinitis pigmentosa to X chromosomal short arm markers. Nussbaum RL; Lewis RA; Lesko JG; Ferrell R Hum Genet; 1985; 70(1):45-50. PubMed ID: 3858218 [TBL] [Abstract][Full Text] [Related]
30. Comprehensive survey of mutations in RP2 and RPGR in patients affected with distinct retinal dystrophies: genotype-phenotype correlations and impact on genetic counseling. Pelletier V; Jambou M; Delphin N; Zinovieva E; Stum M; Gigarel N; Dollfus H; Hamel C; Toutain A; Dufier JL; Roche O; Munnich A; Bonnefont JP; Kaplan J; Rozet JM Hum Mutat; 2007 Jan; 28(1):81-91. PubMed ID: 16969763 [TBL] [Abstract][Full Text] [Related]
31. X-linked dominant cone-rod degeneration: linkage mapping of a new locus for retinitis pigmentosa (RP 15) to Xp22.13-p22.11. McGuire RE; Sullivan LS; Blanton SH; Church MW; Heckenlively JR; Daiger SP Am J Hum Genet; 1995 Jul; 57(1):87-94. PubMed ID: 7611300 [TBL] [Abstract][Full Text] [Related]
32. Genetic analysis of a kindred with X-linked mental handicap and retinitis pigmentosa. Aldred MA; Dry KL; Knight-Jones EB; Hardwick LJ; Teague PW; Lester DH; Brown J; Spowart G; Carothers AD; Raeburn JA Am J Hum Genet; 1994 Nov; 55(5):916-22. PubMed ID: 7977353 [TBL] [Abstract][Full Text] [Related]
33. A retrospective study of registered retinitis pigmentosa patients in The Netherlands. van den Born LI; Bergen AA; Bleeker-Wagemakers EM Ophthalmic Paediatr Genet; 1992 Dec; 13(4):227-36. PubMed ID: 1488223 [TBL] [Abstract][Full Text] [Related]
34. Severe manifestations in carrier females in X linked retinitis pigmentosa. Souied E; Segues B; Ghazi I; Rozet JM; Chatelin S; Gerber S; Perrault I; Michel-Awad A; Briard ML; Plessis G; Dufier JL; Munnich A; Kaplan J J Med Genet; 1997 Oct; 34(10):793-7. PubMed ID: 9350809 [TBL] [Abstract][Full Text] [Related]
35. DNA analysis and recombination in X-linked retinitis pigmentosa. Redmond RM; Graham CA; Craig IW; Nevin NC; Archer DB Eye (Lond); 1990; 4 ( Pt 1)():204-9. PubMed ID: 1969814 [TBL] [Abstract][Full Text] [Related]
36. Prenatal diagnosis of X-linked retinitis pigmentosa (RP) in five pregnancies at risk. Iampieri MP; Mingarelli R; Le Guern E; Novelli G; Dallapiccola B Prenat Diagn; 1994 Apr; 14(4):285-9. PubMed ID: 8066038 [TBL] [Abstract][Full Text] [Related]
37. Genetic linkage between X-linked retinitis pigmentosa and DNA probe DXS7 (L1.28): further linkage data, heterogeneity testing, and risk estimation. Clayton JF; Wright AF; Jay M; McKeown CM; Dempster M; Jay BS; Bird AC; Bhattacharya SS Hum Genet; 1986 Oct; 74(2):168-71. PubMed ID: 2876947 [TBL] [Abstract][Full Text] [Related]
38. X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the X chromosome. Friedrich U; Warburg M; Wieacker P; Wienker TF; Gal A; Ropers HH Hum Genet; 1985; 71(2):93-9. PubMed ID: 2995237 [TBL] [Abstract][Full Text] [Related]
39. Linkage analysis of a large Latin-American family with X-linked retinitis pigmentosa and metallic sheen in the heterozygote carrier. Musarella MA; Anson-Cartwright L; Burghes A; Worton RG; Lesko JG; Nussbaum RL Genomics; 1989 May; 4(4):601-5. PubMed ID: 2568332 [TBL] [Abstract][Full Text] [Related]