126 related articles for article (PubMed ID: 3482421)
1. 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]
2. 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]
3. 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]
4. Radiation-reduced hybrids for the myotonic dystrophy locus.
Brook JD; Zemelman BV; Hadingham K; Siciliano MJ; Crow S; Harley HG; Rundle SA; Buxton J; Johnson K; Almond JW
Genomics; 1992 Jun; 13(2):243-50. PubMed ID: 1612584
[TBL] [Abstract][Full Text] [Related]
5. An informative panel of somatic cell hybrids for physical mapping on human chromosome 19q.
Bachinski LL; Krahe R; White BF; Wieringa B; Shaw D; Korneluk R; Thompson LH; Johnson K; Siciliano MJ
Am J Hum Genet; 1993 Feb; 52(2):375-87. PubMed ID: 8430698
[TBL] [Abstract][Full Text] [Related]
6. A long-range restriction map of the human chromosome 19q13 region: close physical linkage between CKMM and the ERCC1 and ERCC2 genes.
Smeets H; Bachinski L; Coerwinkel M; Schepens J; Hoeijmakers J; van Duin M; Grzeschik KH; Weber CA; de Jong P; Siciliano MJ
Am J Hum Genet; 1990 Mar; 46(3):492-501. PubMed ID: 2309701
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. The physical map of chromosome arm 19q: some new assignments, confirmations and re-assessments.
Brook JD; Knight SJ; Roberts SH; Harley HG; Walsh KV; Rundle SA; Freyne K; Koch MC; Epstein ND; Wieringa B
Hum Genet; 1991 May; 87(1):65-72. PubMed ID: 2037284
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. The syntenic relationship of proximal mouse chromosome 7 and the myotonic dystrophy gene region on human chromosome 19q.
Saunders AM; Seldin MF
Genomics; 1990 Feb; 6(2):324-32. PubMed ID: 2307474
[TBL] [Abstract][Full Text] [Related]
11. Comparative gene mapping: order of loci on the X chromosome is different in mice and humans.
Francke U; Taggart RT
Proc Natl Acad Sci U S A; 1980 Jun; 77(6):3595-9. PubMed ID: 6251472
[TBL] [Abstract][Full Text] [Related]
12. [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma].
Laureys GG
Verh K Acad Geneeskd Belg; 1995; 57(5):389-422. PubMed ID: 8571670
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12.1) in a neuroblastoma patient. Establishment of somatic cell hybrids and identification of PND/A12M2 on chromosome 1 and NF1/SCYA7 on chromosome 17 as breakpoint flanking single copy markers.
Laureys G; Speleman F; Versteeg R; van der Drift P; Chan A; Leroy J; Francke U; Opdenakker G; Van Roy N
Oncogene; 1995 Mar; 10(6):1087-93. PubMed ID: 7700633
[TBL] [Abstract][Full Text] [Related]
15. Assignment of seven genes to distinct intervals on the midportion of human chromosome 19q surrounding the myotonic dystrophy gene region.
Schonk D; van Dijk P; Riegmann P; Trapman J; Holm C; Willcocks TC; Sillekens P; van Venrooij W; Wimmer E; Geurts van Kessel A
Cytogenet Cell Genet; 1990; 54(1-2):15-9. PubMed ID: 1701111
[TBL] [Abstract][Full Text] [Related]
16. A chromosome 19 clone from a translocation breakpoint shows close linkage and linkage disequilibrium with myotonic dystrophy.
Korneluk RG; MacLeod HL; McKeithan TW; Brooks JD; MacKenzie AE
Genomics; 1989 Feb; 4(2):146-51. PubMed ID: 2567698
[TBL] [Abstract][Full Text] [Related]
17. Characterization of a YAC and cosmid contig containing markers tightly linked to the myotonic dystrophy locus on chromosome 19.
Buxton J; Shelbourne P; Davies J; Jones C; Perryman MB; Ashizawa T; Butler R; Brook D; Shaw D; de Jong P
Genomics; 1992 Jul; 13(3):526-31. PubMed ID: 1639381
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. A reordering of human chromosome 19 long-arm DNA markers and identification of markers flanking the myotonic dystrophy locus.
Korneluk RG; MacKenzie AE; Nakamura Y; Dubé I; Jacob P; Hunter AG
Genomics; 1989 Oct; 5(3):596-604. PubMed ID: 2613241
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
