247 related articles for article (PubMed ID: 2877933)
1. Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19.
Shaw DJ; Meredith AL; Sarfarazi M; Harley HG; Huson SM; Brook JD; Bufton L; Litt M; Mohandas T; Harper PS
Hum Genet; 1986 Nov; 74(3):262-6. PubMed ID: 2877933
[TBL] [Abstract][Full Text] [Related]
2. The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locus.
Shaw DJ; Meredith AL; Sarfarazi M; Huson SM; Brook JD; Myklebost O; Harper PS
Hum Genet; 1985; 70(3):271-3. PubMed ID: 2991117
[TBL] [Abstract][Full Text] [Related]
3. Linkage relationships of the protein kinase C gamma gene which exclude it as a candidate for myotonic dystrophy.
Johnson KJ; Jones PJ; Spurr N; Nimmo E; Davies J; Creed H; Weiss M; Williamson R
Cytogenet Cell Genet; 1988; 48(1):13-5. PubMed ID: 2460293
[TBL] [Abstract][Full Text] [Related]
4. Physical and genetic mapping of a novel chromosome 19 ERCC1 marker showing close linkage with myotonic dystrophy.
Shutler G; MacKenzie AE; Brunner H; Wieringa B; de Jong P; Lohman FP; Leblond S; Bailly J; Korneluk RG
Genomics; 1991 Mar; 9(3):500-4. PubMed ID: 1674498
[TBL] [Abstract][Full Text] [Related]
5. Linkage relationships of the insulin receptor gene with the complement component 3, LDL receptor, apolipoprotein C2 and myotonic dystrophy loci on chromosome 19.
Shaw DJ; Meredith AL; Brook JD; Sarfarzi M; Harley HG; Huson SM; Bell GI; Harper PS
Hum Genet; 1986 Nov; 74(3):267-9. PubMed ID: 2877934
[TBL] [Abstract][Full Text] [Related]
6. Genetic and physical demarcation of the locus for dystrophia myotonica.
Wieringa B; Brunner H; Hulsebos T; Schonk D; Ropers HH
Adv Neurol; 1988; 48():47-69. PubMed ID: 2891258
[No Abstract] [Full Text] [Related]
7. Further mapping of markers around the centromere of human chromosome 19.
Brook JD; Skinner M; Roberts SH; Rettig WJ; Almond JW; Shaw DJ
Genomics; 1987 Dec; 1(4):320-8. PubMed ID: 3482421
[TBL] [Abstract][Full Text] [Related]
8. Long-range restriction map of a region of human chromosome 19 containing the apolipoprotein genes, a CLL-associated translocation breakpoint, and two polymorphic MluI sites.
Shaw DJ; Harley HG; Brook JD; McKeithan TW
Hum Genet; 1989 Aug; 83(1):71-4. PubMed ID: 2570021
[TBL] [Abstract][Full Text] [Related]
9. Linkage relationships of the apolipoprotein C1 gene and a cytochrome P450 gene (CYP2A) to myotonic dystrophy.
Walsh KV; Harley HG; Brook JD; Rundle SA; Sarfarazi M; Harper PS; Shaw DJ
Hum Genet; 1990 Aug; 85(3):305-10. PubMed ID: 1975560
[TBL] [Abstract][Full Text] [Related]
10. Localization of a human Na+,K+-ATPase alpha subunit gene to chromosome 19q12----q13.2 and linkage to the myotonic dystrophy locus.
Harley HG; Brook JD; Jackson CL; Glaser T; Walsh KV; Sarfarazi M; Kent R; Lager M; Koch M; Harper PS
Genomics; 1988 Nov; 3(4):380-4. PubMed ID: 2907504
[TBL] [Abstract][Full Text] [Related]
11. Identification of new DNA markers close to the myotonic dystrophy locus.
Brook JD; Harley HG; Walsh KV; Rundle SA; Siciliano MJ; Harper PS; Shaw DJ
J Med Genet; 1991 Feb; 28(2):84-8. PubMed ID: 1672160
[TBL] [Abstract][Full Text] [Related]
12. Three-point linkage analysis employing C3 and 19cen markers assigns the myotonic dystrophy gene to 19q.
Friedrich U; Brunner H; Smeets D; Lambermon E; Ropers HH
Hum Genet; 1987 Mar; 75(3):291-3. PubMed ID: 2881880
[TBL] [Abstract][Full Text] [Related]
13. Definition of subchromosomal intervals around the myotonic dystrophy gene region at 19q.
Schonk D; Coerwinkel-Driessen M; van Dalen I; Oerlemans F; Smeets B; Schepens J; Hulsebos T; Cockburn D; Boyd Y; Davis M
Genomics; 1989 Apr; 4(3):384-96. PubMed ID: 2714797
[TBL] [Abstract][Full Text] [Related]
14. Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19q.
Harley HG; Walsh KV; Rundle S; Brook JD; Sarfarazi M; Koch MC; Floyd JL; Harper PS; Shaw DJ
Hum Genet; 1991 May; 87(1):73-80. PubMed ID: 2037285
[TBL] [Abstract][Full Text] [Related]
15. A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19.
Brunner HG; Smeets H; Lambermon HM; Coerwinkel-Driessen M; van Oost BA; Wieringa B; Ropers HH
Genomics; 1989 Oct; 5(3):589-95. PubMed ID: 2575588
[TBL] [Abstract][Full Text] [Related]
16. Molecular analysis of human muscular dystrophies.
Davies KE; Forrest S; Smith T; Kenwrick S; Ball S; Dorkins H; Patterson M
Muscle Nerve; 1987; 10(3):191-9. PubMed ID: 2882417
[TBL] [Abstract][Full Text] [Related]
17. The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy.
MacKenzie AE; Korneluk RG; Zorzato F; Fujii J; Phillips M; Iles D; Wieringa B; Leblond S; Bailly J; Willard HF
Am J Hum Genet; 1990 Jun; 46(6):1082-9. PubMed ID: 1971150
[TBL] [Abstract][Full Text] [Related]
18. Establishment of the mouse chromosome 7 region with homology to the myotonic dystrophy region of human chromosome 19q.
Cavanna JS; Greenfield AJ; Johnson KJ; Marks AR; Nadal-Ginard B; Brown SD
Genomics; 1990 May; 7(1):12-8. PubMed ID: 1970795
[TBL] [Abstract][Full Text] [Related]
19. Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.
Davies KE; Jackson J; Williamson R; Harper PS; Ball S; Sarfarazi M; Meredith L; Fey G
J Med Genet; 1983 Aug; 20(4):259-63. PubMed ID: 6620325
[TBL] [Abstract][Full Text] [Related]
20. Linkage analysis of the apolipoprotein C2 gene and myotonic dystrophy on human chromosome 19 reveals linkage disequilibrium in a French-Canadian population.
MacKenzie AE; MacLeod HL; Hunter AG; Korneluk RG
Am J Hum Genet; 1989 Jan; 44(1):140-7. PubMed ID: 2562820
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]