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Journal Abstract Search

134 related items for PubMed ID: 2908672

  • 21. Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome.
    Suthers GK, Mulley JC, Voelckel MA, Dahl N, Väisänen ML, Steinbach P, Glass IA, Schwartz CE, van Oost BA, Thibodeau SN.
    Am J Hum Genet; 1991 Mar; 48(3):460-7. PubMed ID: 1671806
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  • 25. Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions.
    Connor JM, Pirrit LA, Yates JR, Crossley JA, Imrie SJ, Colgan JM.
    J Med Genet; 1987 Jan; 24(1):14-22. PubMed ID: 2879932
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  • 26. X-linked lymphoproliferative disease: linkage studies using DNA probes.
    Harris A, Lenoir GM, Lankester SA.
    Clin Genet; 1988 Mar; 33(3):162-8. PubMed ID: 2896078
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  • 29. Choroideremia-locus maps between DXS3 and DXS11 on Xq.
    Gal A, Brunsmann F, Hogenkamp D, Rüther K, Ahlert D, Wienker TF, Hammerstein W, Pawlowitzki IH.
    Hum Genet; 1986 Jun; 73(2):123-6. PubMed ID: 3755117
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  • 30. Linkage relationships of X-linked choroideremia to DXYS1 and DXS3.
    MacDonald IM, Sandre RM, Wong P, Hunter AG, Tenniswood MP.
    Hum Genet; 1987 Nov; 77(3):233-5. PubMed ID: 2890569
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  • 32. DNA analysis and recombination in X-linked retinitis pigmentosa.
    Redmond RM, Graham CA, Craig IW, Nevin NC, Archer DB.
    Eye (Lond); 1990 Nov; 4 ( Pt 1)():204-9. PubMed ID: 1969814
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  • 35. Genetic linkage studies of X-linked hypophosphataemic rickets in a Saudi Arabian family.
    Thakker RV, Farmery MR, Sakati NA, Milner RD.
    Clin Endocrinol (Oxf); 1992 Oct; 37(4):338-43. PubMed ID: 1483289
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  • 36. Assignment of the X-linked torsion dystonia gene to Xq21 by linkage analysis.
    Kupke KG, Lee LV, Müller U.
    Neurology; 1990 Sep; 40(9):1438-42. PubMed ID: 1975433
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  • 37. Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp.
    Gal A, Schinzel A, Orth U, Fraser NA, Mollica F, Craig IW, Kruse T, Mächler M, Neugebauer M, Bleeker-Wagemakers LM.
    Hum Genet; 1989 Mar; 81(4):315-8. PubMed ID: 2564836
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  • 39. Molecular basis of Fabry disease: mutations and polymorphisms in the human alpha-galactosidase A gene.
    Eng CM, Desnick RJ.
    Hum Mutat; 1994 Mar; 3(2):103-11. PubMed ID: 7911050
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  • 40. Gene mapping of X-linked choroideremia with restriction fragment-length polymorphisms.
    MacDonald IM, Sandre RM, Hunter AG, Tenniswood MP.
    Can J Ophthalmol; 1987 Oct; 22(6):310-5. PubMed ID: 2892583
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