101 related articles for article (PubMed ID: 3016653)
1. RFLPs at the D19S19 locus of human chromosome 19 linked to myotonic dystrophy (DM).
Roses AD; Pericak-Vance MA; Ross DA; Yamaoka L; Bartlett RJ
Nucleic Acids Res; 1986 Jul; 14(13):5569. PubMed ID: 3016653
[No 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. Gene mapping and myotonic dystrophy.
Harper PS; Shaw D; Meredith L; Sarfarazi M; Brook D; Huson S
Prog Clin Biol Res; 1985; 177():61-76. PubMed ID: 2989839
[No Abstract] [Full Text] [Related]
4. Myotonic dystrophy and gene mapping on human chromosome 19.
Brook JD; Shaw DJ; Meredith AL
Biotechnol Genet Eng Rev; 1985; 3():311-47. PubMed ID: 3004536
[No Abstract] [Full Text] [Related]
5. 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]
6. 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]
7. Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19q.
Johnson K; Nimmo E; Jones P; Weiss M; Savontaus ML; Anvret M; Bartlett R; Roses A; Shaw D; Harper PS
Hum Genet; 1988 Dec; 80(4):379-81. PubMed ID: 3198115
[TBL] [Abstract][Full Text] [Related]
8. Localization of cloned unique DNA to three different regions of chromosome 19: screen for linkage probes for myotonic dystrophy.
Yamaoka LH; Bartlett RJ; Ross DA; Fey GH; Ledbetter DH; Bruns G; Pericak-Vance MA; Herbstreith MH; Roses AD
J Neurogenet; 1985 Dec; 2(6):403-12. PubMed ID: 3001264
[TBL] [Abstract][Full Text] [Related]
9. The locus for Japanese myotonic dystrophy is also linked to D19S19 on the long arm of chromosome 19.
Takemoto Y; Miki T; Nishikawa K; Nakura J; Kamino K; Takai S; Honjo T; Ogihara T
Genomics; 1990 Jan; 6(1):195-6. PubMed ID: 2303261
[No Abstract] [Full Text] [Related]
10. A new probe for the diagnosis of myotonic muscular dystrophy.
Bartlett RJ; Pericak-Vance MA; Yamaoka L; Gilbert J; Herbstreith M; Hung WY; Lee JE; Mohandas T; Bruns G; Laberge C
Science; 1987 Mar; 235(4796):1648-50. PubMed ID: 3029876
[TBL] [Abstract][Full Text] [Related]
11. Recombination events that locate myotonic dystrophy distal to APOC2 on 19q.
Johnson K; Shelbourne P; Davies J; Buxton J; Nimmo E; Anvret M; Bonduelle M; Williamson B; Savontaus ML
Genomics; 1989 Nov; 5(4):746-51. PubMed ID: 2591962
[TBL] [Abstract][Full Text] [Related]
12. Exclusion of the C3 gene from the 19q133 to 19qter region by Southern analysis of human-rodent somatic cell hybrids, employing a cloned genomic C3 gene fragment.
Wieacker P; Fey G; Voiculescu I; Ropers HH
Acta Anthropogenet; 1983; 7(2):107-12. PubMed ID: 6331467
[TBL] [Abstract][Full Text] [Related]
13. Preclinical detection in Japanese families with myotonic dystrophy using polymorphic DNA markers.
Takemoto Y; Miki T; Nakura J; Nishikawa K; Kamino K; Takeda S; Kuzu K; Osame M; Nakagawa M; Higuchi I
Jinrui Idengaku Zasshi; 1989 Sep; 34(3):189-94. PubMed ID: 2576756
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Linkage analysis of peripheral neurofibromatosis (Von Recklinghausen disease) and chromosome 19 markers linked to myotonic dystrophy.
Huson SM; Meredith AL; Sarfarazi M; Shaw DJ; Compston DA; Harper PS
J Med Genet; 1986 Feb; 23(1):55-7. PubMed ID: 3081725
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. [The RFLP of LDR152/PstI in the Chinese and its application to linkage analysis in a myotonic dystrophy family].
Tan J; Qiu XF; Xue JL; Liu ZD; Li YS; Zai CH
Yi Chuan Xue Bao; 1991; 18(1):6-11. PubMed ID: 1674205
[TBL] [Abstract][Full Text] [Related]
19. Genetic mapping of a second myotonic dystrophy locus.
Ranum LP; Rasmussen PF; Benzow KA; Koob MD; Day JW
Nat Genet; 1998 Jun; 19(2):196-8. PubMed ID: 9620781
[TBL] [Abstract][Full Text] [Related]
20. A Bgl II polymorphism detected by LDR152 [D19S19].
Walker AP; Bartlett RJ; Yamaoka LH; Secore SL; Lee JE; Gilbert J; Herbstreith M; Pericak-Vance MA; Hung WY; Roses AD
Nucleic Acids Res; 1988 Sep; 16(18):9063. PubMed ID: 2902564
[No Abstract] [Full Text] [Related]
[Next] [New Search]