142 related articles for article (PubMed ID: 1684562)
41. Genetic heterogeneity in X-linked amelogenesis imperfecta.
Aldred MJ; Crawford PJ; Roberts E; Gillespie CM; Thomas NS; Fenton I; Sandkuijl LA; Harper PS
Genomics; 1992 Nov; 14(3):567-73. PubMed ID: 1358807
[TBL] [Abstract][Full Text] [Related]
42. Linkage mapping of highly informative DNA polymorphisms within the human interferon-alpha receptor gene on chromosome 21.
McInnis MG; Lutfalla G; Slaugenhaupt S; Petersen MB; Uze G; Chakravarti A; Antonarakis SE
Genomics; 1991 Nov; 11(3):573-6. PubMed ID: 1685477
[TBL] [Abstract][Full Text] [Related]
43. Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal marker.
Hanauer A; Alembik Y; Arveiler B; Formiga L; Gilgenkrantz S; Mandel JL
Hum Genet; 1988 Oct; 80(2):177-80. PubMed ID: 2902000
[TBL] [Abstract][Full Text] [Related]
44. Genetic mapping of X linked ocular albinism: linkage analysis in British families.
Charles SJ; Moore AT; Yates JR
J Med Genet; 1992 Aug; 29(8):552-4. PubMed ID: 1355560
[TBL] [Abstract][Full Text] [Related]
45. Autosomal dominant progressive nephropathy with deafness: linkage to a new locus on chromosome 11q24.
Prakash S; Chung KW; Sinha S; Barmada M; Ellis D; Ferrell RE; Finegold DN; Randhawa PS; Dinda A; Vats A
J Am Soc Nephrol; 2003 Jul; 14(7):1794-803. PubMed ID: 12819239
[TBL] [Abstract][Full Text] [Related]
46. Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia.
Schwartz M; Yang HM; Niebuhr E; Rosenberg T; Page DC
Hum Genet; 1988 Feb; 78(2):156-60. PubMed ID: 3422216
[TBL] [Abstract][Full Text] [Related]
47. [X-linked thin basement membrane nephropathy was linked with COL4A5 gene].
Zhang C; Zhu S; Zhang Y
Zhonghua Yi Xue Za Zhi; 2000 Aug; 80(8):582-4. PubMed ID: 11798821
[TBL] [Abstract][Full Text] [Related]
48. Genetic heterogeneity in X-linked agammaglobulinemia complicates carrier detection and prenatal diagnosis.
Mensink EJ; Thompson A; Schot JD; Kraakman ME; Sandkuyl LA; Schuurman RK
Clin Genet; 1987 Feb; 31(2):91-6. PubMed ID: 2881637
[TBL] [Abstract][Full Text] [Related]
49. X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis.
Zonana J; Clarke A; Sarfarazi M; Thomas NS; Roberts K; Marymee K; Harper PS
Am J Hum Genet; 1988 Jul; 43(1):75-85. PubMed ID: 3163892
[TBL] [Abstract][Full Text] [Related]
50. Linkage relationship between retinoschisis and four marker loci.
Gellert G; Peterson J; Krawczak M; Zoll B
Hum Genet; 1988 Aug; 79(4):382-4. PubMed ID: 2900804
[TBL] [Abstract][Full Text] [Related]
51. Gene localisation of X-linked hypohidrotic ectodermal dysplasia (C-S-T syndrome).
MacDermot KD; Winter RM; Malcolm S
Hum Genet; 1986 Oct; 74(2):172-3. PubMed ID: 3464559
[TBL] [Abstract][Full Text] [Related]
52. Segregation of hematuria in thin basement membrane disease with haplotypes at the loci for Alport syndrome.
Buzza M; Wilson D; Savige J
Kidney Int; 2001 May; 59(5):1670-6. PubMed ID: 11318937
[TBL] [Abstract][Full Text] [Related]
53. Genetic linkage mapping of the CYP11A1 gene encoding the cholesterol side-chain cleavage P450scc close to the CYP1A1 gene and D15S204 in the chromosome 15q22.33-q23 region.
Durocher F; Morissette J; Simard J
Pharmacogenetics; 1998 Feb; 8(1):49-53. PubMed ID: 9511181
[TBL] [Abstract][Full Text] [Related]
54. Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14.
Mulley JC; Gedeon AK; Thorn KA; Bates LJ; Sutherland GR
Am J Med Genet; 1987 Jun; 27(2):435-48. PubMed ID: 2886048
[TBL] [Abstract][Full Text] [Related]
55. The Wiskott-Aldrich syndrome: refinement of the localization on Xp and identification of another closely linked marker locus, OATL1.
Greer WL; Peacocke M; Siminovitch KA
Hum Genet; 1992 Feb; 88(4):453-6. PubMed ID: 1346773
[TBL] [Abstract][Full Text] [Related]
56. Multipoint linkage analysis in X-linked juvenile retinoschisis.
Bergen AA; van Schooneveld MJ; Orth U; Bleeker-Wagemakers EM; Gal A
Clin Genet; 1993 Mar; 43(3):113-6. PubMed ID: 8500256
[TBL] [Abstract][Full Text] [Related]
57. Tightly linked flanking markers for the Lowe oculocerebrorenal syndrome, with application to carrier assessment.
Reilly DS; Lewis RA; Ledbetter DH; Nussbaum RL
Am J Hum Genet; 1988 May; 42(5):748-55. PubMed ID: 2895982
[TBL] [Abstract][Full Text] [Related]
58. Three DNA markers for hypophosphataemic rickets.
Rowe PS; Read AP; Mountford R; Benham F; Kruse TA; Camerino G; Davies KE; O'Riordan JL
Hum Genet; 1992 Jul; 89(5):539-42. PubMed ID: 1353055
[TBL] [Abstract][Full Text] [Related]
59. Substitution of A1498D in noncollagen domain of a5(IV) collagen chain associated with adult-onset X-linked Alport syndrome.
Tverskaya S; Bobrynina V; Tsalykova F; Ignatova M; Krasnopolskaya X; Evgrafov O
Hum Mutat; 1996; 7(2):149-50. PubMed ID: 8829632
[No Abstract] [Full Text] [Related]
60. Mapping the mutation causing the X-linked lymphoproliferative syndrome in relation to restriction fragment length polymorphisms on Xq.
Skare JC; Sullivan JL; Milunsky A
Hum Genet; 1989 Jul; 82(4):349-53. PubMed ID: 2567695
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
