Multipoint linkage analysis and homogeneity tests in 15 Dutch X-linked retinitis pigmentosa families

References

• Bird A C. X-linked retinitis pigmentosa. Br J Ophthalmol 1975; 59: 177–199
   PubMed Web of Science ®Google Scholar
• Bhattacharya S S, Wright A F, Clayton J F, Price W H, Phillips C I, McKeown C ME, Jay M, Bird J M, Pearson P L, Southern E M, Evans H J. Close linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant dna probe L1.28. Nature (London) 1984; 309: 253–255
   PubMedGoogle Scholar
• Friedrich U, Warburg M, Wieacker P, Wienker T F, Gal A, Ropers H-H. X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the human X chromosome. Hum Genet 1985; 71: 93–99
   PubMedGoogle Scholar
• Wright A F, Bhattacharya S S, Clayton J F, Dempster M, Tippet P, McKeown C ME, Jay M. Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers. Exclusion of the disease locus from Xp21.1 and localization to between dxs 7 and dxs 14. Am J Hum Genet 1987; 41: 635–644
   PubMedGoogle Scholar
• Denton M J, Chen J D, Serravalle S, Colley P, Halladay F B, Donald J. Analysis of linkage relationships of X-linked retinitis pigmentosa with the following Xp loci: L1.28, otc, 754, XJ-1, pert87, and C7. Hum Genet 1988; 78: 60–64
   PubMedGoogle Scholar
• Ott J, Bhattacharya S S, Chen J D, Denton M J, Donald J, Dubay C, Farrar G J. Localizing multiple X chromosome linked retinitis pigmentosa loci using multilocus homogeneity tests. Proc Natl Acad Sci usa 1990; 87: 701–704
   PubMed Web of Science ®Google Scholar
• Musarella M A, Burghes A, Anson-Cartwright L, Mahtani M M, Argonza R, Tsui L C, Worton R. Localization of the gene for X-linked recessive type of retinitis pigmentosa (xlrp) to Xp21 by linkage analysis. Am J Hum Genet 1988; 43: 484–494
   PubMedGoogle Scholar
• Wirth B, Denton M J, Chen J-D, Neugebauer M, Halliday F B, Van Schooneveld M, Bleeker-Wagemakers E M. Two different genes for X-linked retinitis pigmentosa. Genomics 1988; 2: 263–266
   PubMedGoogle Scholar
• Meitinger T, Fraser N A, Lorenz B, Zrenner E, Murken J, Craig I W. Linkage of X-linked retinitis pigmentosa to the hypervariable DNA marker M27-beta (DXS255). Hum Genet 1989; 81: 283–286
   PubMedGoogle Scholar
• Coleman M, Bhattacharya S, Lindsay S, Wright A, Jay M, Litt M, Craig I, Davies K. Localization of the micro-satellite probe dxs426 between dxs7 and dxs255 on Xp and linkage to retinitis pigmentosa. Am J Hum Genet 1990; 47: 935–940
   PubMedGoogle Scholar
• Musarella M A, Anson-Cartwright L, Leal S M, Gilbert L D, Worton R G, Fishman G A, Ott J. Multipoint linkage analysis and heterogeneity testing in 20 X-linked retinitis pigmentosa families. Genomics 1990; 8: 286–296
   PubMed Web of Science ®Google Scholar
• Born L I, Bergen A AB, Bleeker-Wagemakers E M. A retrospective study of registered X-linked retinitis pigmentosa patients in the Netherlands. Ophthalmic Paediatr Genet 1992; 13(4)227–236
   PubMedGoogle Scholar
• Fishman G A, Weinberg A B, McMahon T T. X-linked retinitis pigmentosa: clinical characteristics of carriers. Arch Ophthalmol 1990; 104: 1329–1335
   Google Scholar
• Bergen A AB, Samanns C, Schuurman E JM, Van Osch L, Van Dorp D B, Pinckers A JGL, Bakker E, Gal A, Van Ommen G JB, Bleeker-Wagemakers E M. Multipoint linkage analysis in X-linked albinism of the Nettleship-Falls type. Hum Genet 1991; 88: 162–166
   PubMed Web of Science ®Google Scholar
• Bergen A AB, Wapenaar M C, Schuurman E JM, Diergaarde P J, Lerach H, Monaco A P, Bakker E, Bleeker-Wagemakers E M, Van Ommen G JB. Detection of a new submicroscopic Norrie disease deletion interval with a novel DNA probe isolated by differential ALU-PCR fingerprint cloning. Cytogenet Cell Genet 1993; 62: 231–235
   PubMedGoogle Scholar
• Davies K E, Mandel J L, Monaco A P, Nussbaum R L, Willard H F. Report of the Committee of the genetic constitution of the X chromosome: HGM 10.5 Oxford. Cytogenet Cell Genet 1990; 51: 1–4, 397, 502
   Google Scholar
• Van Dorp D B, Wright A F, Carothers A D, Bleeker-Wagemakers E M. A family with rp3 type of X-linked retinitis pigmentosa: an association with ciliary abnormalities. Hum Genet 1992; 88: 331–334
   PubMed Web of Science ®Google Scholar
• Lathrop G M, Lalouel J M. Easy calculation of Lod scores and genetic risks on small computers. Proc Natl Acad Sci USA 1984; 74: 1245–1249
   Google Scholar
• Ott J. Variability of the recombination fraction. Analysis of Human Genetic Linkage. Johns Hopkins University Press, Baltimore 1985; 97–119
   Google Scholar
• Teague P W, Aldred M A, Jay M, Dempster M, Harrison, Carothers A D, Hardwick L J, Evans H J, Strain L, Brock D JH, Bundy D, Jay B, Bird A C, Bhattacharya S S, Wright A F. Heterogeneity analysis in 40 X-linked retinitis pigmentosa families. Am J Hum Genet 1994; 55: 105-m
   Google Scholar
• Aldred M A, Teague P W, Jay M, Bundey S, Redmond R M, Jay B, Bird A C, Bhattacharya S S, Wright A F. Retinitis pigmentosa families showing apparent X-linked inheritance, but unlinked to the rp2 or rp3 loci. J Med Gen 1994; 31: 848–852
   PubMedGoogle Scholar
• Wright A F, Bhattacharya S S, Craig I W, Jay M, Dempster M, Fraser N, Meitinger T. Recombinant mapping of retinitis pigmentosa genes. Molecular Biology of the Eye: Genes, Vision and Ocular Disease, A Wright, B Jay. Alan R. Liss, Inc., New York 1988; 293–303
   Google Scholar
• Jacobson S G, Roman A J, Cideciyan A V, Robey G R, Iwata T, Inana G. X-linked retinitis pigmentosa: functional phenotype of an rp2 genotype. Invest Ophthalm Vis Sci 1992; 33: 13, 3481–3492
   Google Scholar
• Boughman J, Fishman G A. A genetic analysis of retinitis pigmentosa. Br J Ophthalmol 1983; 67: 449–454
   PubMed Web of Science ®Google Scholar
• Edwards J H. The population genetics of Duchenne: natural and artificial selection in Duchenne muscular dystrophy. J Med Genet 1986; 23: 521–530
   PubMedGoogle Scholar
• Weeks D E, Ott J. Risk calculations under heterogeneity. Am J Hum Genet 1989; 45: 817–821
   Google Scholar
• Bergen A AB, Platje E JM, Craig I, Bakker E, Bleeker-Wagemakers E M, Van Ommen G JB. Carrier detection in X-linked retinitis pigmentosa by multipoint DNA analysis: problems due to genetic heterogeneity. Ophthalmic Paediatr Genet 1991; 12(2)99–103
   PubMed Web of Science ®Google Scholar