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Journal Abstract Search

163 related items for PubMed ID: 2904400

  • 21. Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13-q21 deletion related deafness.
    Reardon W, Roberts S, Phelps PD, Thomas NS, Beck L, Issac R, Hughes HE.
    Am J Med Genet; 1992 Nov 01; 44(4):513-7. PubMed ID: 1442898
    [Abstract] [Full Text] [Related]

  • 22. Linkage relationship between retinoschisis and four marker loci.
    Gellert G, Peterson J, Krawczak M, Zoll B.
    Hum Genet; 1988 Aug 01; 79(4):382-4. PubMed ID: 2900804
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  • 23. Close linkage of a gene for X linked deafness to three microsatellite repeats at Xq21 in radiologically normal and abnormal families.
    Bitner-Glindzicz M, de Kok Y, Summers D, Huber I, Cremers FP, Ropers HH, Reardon W, Pembrey ME, Malcolm S.
    J Med Genet; 1994 Dec 01; 31(12):916-21. PubMed ID: 7891371
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  • 24. DNA linkage analysis of X-linked retinoschisis.
    Dahl N, Goonewardena P, Chotai J, Anvret M, Pettersson U.
    Hum Genet; 1988 Mar 01; 78(3):228-32. PubMed ID: 2894345
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  • 25. A multipedigree linkage study of X-linked deafness: linkage to Xq13-q21 and evidence for genetic heterogeneity.
    Reardon W, Middleton-Price HR, Sandkuijl L, Phelps P, Bellman S, Luxon L, Pembrey ME, Malcolm S.
    Genomics; 1991 Dec 01; 11(4):885-94. PubMed ID: 1783396
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  • 26. X-linked deafness with stapes gusher in females.
    Papadaki E, Prassopoulos P, Bizakis J, Karampekios S, Papadakis H, Gourtsoyiannis N.
    Eur J Radiol; 1998 Nov 01; 29(1):71-5. PubMed ID: 9934561
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  • 28. Regional localization of the phosphoglycerate kinase gene and pseudogene on the human X chromosome and assignment of a related DNA sequence to chromosome 19.
    Willard HF, Goss SJ, Holmes MT, Munroe DL.
    Hum Genet; 1985 Nov 01; 71(2):138-43. PubMed ID: 2995234
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  • 30. A new mutation in the POU3F4 gene in a Japanese family with X-linked mixed deafness (DFN3).
    Hagiwara H, Tamagawa Y, Kitamura K, Kodera K.
    Laryngoscope; 1998 Oct 01; 108(10):1544-7. PubMed ID: 9778298
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  • 31. Linkage of PGK1 to X-linked severe combined immunodeficiency (IMD4) allows predictive testing in families with no surviving male.
    Goodship J, Levinsky R, Malcolm S.
    Hum Genet; 1989 Dec 01; 84(1):11-4. PubMed ID: 2606471
    [Abstract] [Full Text] [Related]

  • 32. Multipoint linkage analysis in X-linked juvenile retinoschisis.
    Bergen AA, van Schooneveld MJ, Orth U, Bleeker-Wagemakers EM, Gal A.
    Clin Genet; 1993 Mar 01; 43(3):113-6. PubMed ID: 8500256
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  • 33. Multipoint linkage analysis of loci in the proximal long arm of the human X chromosome: application to mapping the choroideremia locus.
    Lesko JG, Lewis RA, Nussbaum RL.
    Am J Hum Genet; 1987 Apr 01; 40(4):303-11. PubMed ID: 2883887
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  • 34. Confirmation of X-linked inheritance and provisional mapping of the keratosis follicularis spinulosa decalvans gene on Xp in a large Dutch family.
    Oosterwijk JC, Nelen M, Van Zandvoort PM, Van Osch LD, Oranje AP, Wittebol-Post D, Van Oost BA.
    Ophthalmic Paediatr Genet; 1992 Mar 01; 13(1):27-30. PubMed ID: 1350668
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  • 35. Deletion mapping of X-linked mixed deafness (DFN3) identifies a 265-525-kb region centromeric of DXS26.
    Dahl N, Laporte J, Hu L, Biancalana V, Le Palier D, Cohen D, Piussan C, Mandel JL.
    Am J Hum Genet; 1995 Apr 01; 56(4):999-1002. PubMed ID: 7717411
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  • 39. Chromosomal localization of phosphoglycerate kinase (PGK) gene in Candida albicans using a heterologous probe.
    Manavathu EK.
    Indian J Exp Biol; 1993 Mar 01; 31(3):206-9. PubMed ID: 8099062
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