173 related articles for article (PubMed ID: 7276965)
21. Autosomal dominant spinocerebellar ataxia: locus heterogeneity in a Nebraska kindred.
Ranum LP; Rich SS; Nance MA; Duvick LA; Aita JF; Orr HT; Anton-Johnson S; Schut LJ
Neurology; 1992 Feb; 42(2):344-7. PubMed ID: 1736163
[TBL] [Abstract][Full Text] [Related]
22. Non-association of Friedreich's ataxia and HLA based on five families.
Chamberlain S; Walker JL; Sachs JA; Wolf E; Festenstein H
Can J Neurol Sci; 1979 Nov; 6(4):451-2. PubMed ID: 543986
[No Abstract] [Full Text] [Related]
23. Amish study, IV: Genetic linkage study of pedigrees of bipolar probands.
Kidd KK; Egeland JA; Molthan L; Pauls DL; Kruger SD; Messner KH
Am J Psychiatry; 1984 Sep; 141(9):1042-8. PubMed ID: 6331772
[TBL] [Abstract][Full Text] [Related]
24. Friedreich ataxia in Italian families: genetic homogeneity and linkage disequilibrium with the marker loci D9S5 and D9S15.
Pandolfo M; Sirugo G; Antonelli A; Weitnauer L; Ferretti L; Leone M; Dones I; Cerino A; Fujita R; Hanauer A
Am J Hum Genet; 1990 Aug; 47(2):228-35. PubMed ID: 2378348
[TBL] [Abstract][Full Text] [Related]
25. Genetic recombination events which position the Friedreich ataxia locus proximal to the D9S15/D9S5 linkage group on chromosome 9q.
Chamberlain S; Farrall M; Shaw J; Wilkes D; Carvajal J; Hillerman R; Doudney K; Harding AE; Williamson R; Sirugo G
Am J Hum Genet; 1993 Jan; 52(1):99-109. PubMed ID: 8434613
[TBL] [Abstract][Full Text] [Related]
26. A family segregating a Friedreich ataxia phenotype that is not linked to the FRDA locus.
Smeyers P; Monrós E; Vílchez J; Lopez-Arlandis J; Prieto F; Palau F
Hum Genet; 1996 Jun; 97(6):824-8. PubMed ID: 8641704
[TBL] [Abstract][Full Text] [Related]
27. Prenatal diagnosis of Friedreich ataxia.
Wallis J; Shaw J; Wilkes D; Farrall M; Williamson R; Chamberlain S; Skare JC; Milunsky A
Am J Med Genet; 1989 Nov; 34(3):458-61. PubMed ID: 2574535
[TBL] [Abstract][Full Text] [Related]
28. Hereditary ataxia and the sixth chromosome.
Koeppen AH; Goedde HW; Hiller C; Hirth L; Benkmann HG
Arch Neurol; 1981 Mar; 38(3):158-64. PubMed ID: 6937161
[TBL] [Abstract][Full Text] [Related]
29. Adult onset spinocerebellar ataxia linked to HLA in a South African kindred of mixed ancestry.
Bryer A; Martell RW; du Toit ED; Beighton P
Tissue Antigens; 1992 Sep; 40(3):111-5. PubMed ID: 1440565
[TBL] [Abstract][Full Text] [Related]
30. Close genetic linkage between diabetes mellitus and kidd blood group.
Hodge SE; Anderson CE; Neiswanger K; Field LL; Spence MA; Sparkes RS; Sparkes MC; Crist M; Terasaki PI; Rimoin DL; Rotter JI
Lancet; 1981 Oct; 2(8252):893-5. PubMed ID: 6117683
[TBL] [Abstract][Full Text] [Related]
31. Late onset autosomal dominant cerebellar ataxia. A family description and linkage analysis with the HLA system.
Arruda WO; Petzl-Erler ML; Cardoso MA; Lehner T; Ott J
Arq Neuropsiquiatr; 1991 Sep; 49(3):285-91. PubMed ID: 1807228
[TBL] [Abstract][Full Text] [Related]
32. Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typing.
Jackson JF; Currier RD; Terasaki PI; Morton NE
N Engl J Med; 1977 May; 296(20):1138-41. PubMed ID: 857157
[TBL] [Abstract][Full Text] [Related]
33. [A clinical study of a family affected with HLA-linked hereditary spinocerebellar ataxia].
Sasaki H; Hamada T; Wakisaka A; Tashiro K
No To Shinkei; 1990 Nov; 42(11):1103-11. PubMed ID: 2076357
[TBL] [Abstract][Full Text] [Related]
34. Identification of a hypervariable microsatellite polymorphism within D9S15 tightly linked to Friedrich's ataxia.
Wallis J; Williamson R; Chamberlain S
Hum Genet; 1990 Jun; 85(1):98-100. PubMed ID: 2358306
[TBL] [Abstract][Full Text] [Related]
35. The inheritance of immunoglobulin E: genetic linkage analysis.
Meyers DA; Hasstedt SJ; Marsh DG; Skolnick M; King MC; Bias WB; Amos DB
Am J Med Genet; 1983 Dec; 16(4):575-81. PubMed ID: 6581721
[TBL] [Abstract][Full Text] [Related]
36. Exclusion mapping of the hereditary dentatorubropallidoluysian atrophy gene from the Huntington's disease locus.
Kondo I; Ohta H; Yazaki M; Ikeda JE; Gusella JF; Kanazawa I
J Med Genet; 1990 Feb; 27(2):105-8. PubMed ID: 1969487
[TBL] [Abstract][Full Text] [Related]
37. A linkage study of acrokeratoelastoidosis. Possible mapping to chromosome 2.
Greiner J; Krüger J; Palden L; Jung EG; Vogel F
Hum Genet; 1983; 63(3):222-7. PubMed ID: 6221990
[TBL] [Abstract][Full Text] [Related]
38. No evidence for linkage between the loci for coagulation factor XIII-A and HLA.
Nishigaki T; Tokunaga K; Ishii C; Omoto K; Akaza T; Akiyama N; Juji T; Murata S; Naito S; Saji H
Hum Genet; 1986 Mar; 72(3):266-7. PubMed ID: 2870019
[TBL] [Abstract][Full Text] [Related]
39. HLA and epidermolysis bullosa: evidence for independent assortment of Weber-Cockayne subtype of epidermolysis bullosa and HLA complex.
Vaidya S; Tyring SK; Feldkamp M; Johnson LB; Fine JD
J Dermatol Sci; 1991 May; 2(3):155-60. PubMed ID: 1878343
[TBL] [Abstract][Full Text] [Related]
40. Hereditary malignant melanoma is not linked to the HLA complex on chromosome 6.
Bale SJ; Greene MH; Murray C; Goldin LR; Johnson AH; Mann D
Int J Cancer; 1985 Oct; 36(4):439-43. PubMed ID: 4044054
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
