D19S51 IS CLOSELY LINKED WITH AND MAPS DISTAL TO THE MYOTONIC-DYSTROPHY LOCUS ON 19Q

被引:0
|
作者
TSILFIDIS, C
MACKENZIE, AE
SHUTLER, G
LEBLOND, S
BAILLY, J
JOHNSON, K
WILLIAMSON, R
SIEGELBARTELT, J
KORNELUK, RG
机构
[1] CHILDRENS HOSP EASTERN ONTARIO,DIV GENET,401 SMYTH RD,OTTAWA K1H 8L1,ONTARIO,CANADA
[2] UNIV OTTAWA,DEPT PEDIAT,OTTAWA K1N 6N5,ONTARIO,CANADA
[3] HOSP SICK CHILDREN,DEPT CLIN GENET,TORONTO M5G 1X8,ONTARIO,CANADA
[4] CHARING CROSS & WESTMINSTER MED SCH,DEPT ANAT,LONDON,ENGLAND
[5] ST MARYS HOSP,SCH MED,DEPT BIOCHEM & MOLEC GENET,LONDON,ENGLAND
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Recent genetic linkage studies have mapped the myotonic dystrophy (DM) locus to 19ql3.3. All closely linked DM markers identified to date have been located on the centromeric side of the disease locus, with a relatively large genetic interval (9 cM) observed between the nearest distal marker and DM. We show here that the recently described marker p134C is tightly linked to DM (peak lod score 35.8 at peak recombination fraction .006) and confirm the previous suggestion that the p134C locus, D19S51 maps distal to the disease locus. D19S51 and the closest proximal flanking loci, ERCC1 and D19S115 (pE0.8), define a small genetic interval of less than 2 cM that contains the DM locus.
引用
收藏
页码:961 / 965
页数:5
相关论文
共 50 条
  • [21] A new family of Greek origin maps to the CRD locus for autosomal dominant cone-rod dystrophy on 19q
    Papaioannou, M
    Bessant, D
    Payne, A
    Bellingham, J
    Rougas, C
    Loutradis-Anagnostou, A
    Gregory-Evans, C
    Balassopoulou, A
    Bhattacharya, S
    JOURNAL OF MEDICAL GENETICS, 1998, 35 (05) : 429 - 431
  • [22] Suggestive linkage of an autosomal dominant cataract locus (ADC 51) to chromosome 19q
    Turner, JL
    Richter, L
    Flodman, P
    Chamberlain, W
    von-Bischhoffshausen, FRB
    Spence, MA
    Bateman, JB
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2003, 44 : U301 - U301
  • [23] LINKAGE MAP AROUND THE MYOTONIC-DYSTROPHY LOCUS AND EVIDENCE FOR A CHARCOT MARIE TOOTH NEUROPATHY LOCUS ON CHROMOSOME-19
    BRUNNER, H
    SMEETS, H
    COERWINKELDRIESSEN, M
    VANOOST, BA
    SPAANS, F
    WIERINGA, B
    ROPERS, HH
    CYTOGENETICS AND CELL GENETICS, 1989, 51 (1-4): : 971 - 971
  • [24] A NEW POLYMORPHIC PROBE WHICH DEFINES THE REGION OF CHROMOSOME-19 CONTAINING THE MYOTONIC-DYSTROPHY LOCUS
    JOHNSON, K
    SHELBOURNE, P
    DAVIES, J
    BUXTON, J
    NIMMO, E
    SICILIANO, MJ
    BACHINSKI, LL
    ANVRET, M
    HARLEY, H
    RUNDLE, S
    MIKI, T
    BRUNNER, H
    WILLIAMSON, R
    AMERICAN JOURNAL OF HUMAN GENETICS, 1990, 46 (06) : 1073 - 1081
  • [25] Coincidence or association? Two 19q disorders in the same patient: 1p/19q co-deleted oligodendroglioma and myotonic dystrophy type 1
    Grewal, Jai
    Kallio, Merja
    Tummala, Sudhakar
    Puduvalli, Vinay
    NEURO-ONCOLOGY, 2007, 9 (04) : 546 - 547
  • [26] MYOTONIA CONGENITA (THOMSENS DISEASE) EXCLUDED FROM THE REGION OF THE MYOTONIC-DYSTROPHY LOCUS ON CHROMOSOME-19
    KOCH, M
    HARLEY, H
    SARFARAZI, M
    BENDER, K
    WIENKER, T
    ZOLL, B
    HARPER, PS
    HUMAN GENETICS, 1989, 82 (02) : 163 - 166
  • [27] A RECOMBINATION EVENT IN A MYOTONIC-DYSTROPHY PATIENT THAT LOCATES THE 2 MOST TIGHTLY LINKED MARKERS ON THE SAME SIDE OF THE DEFECT LOCUS ON CHROMOSOME-19
    JOHNSON, K
    JONES, P
    NIMMO, E
    WEISS, M
    MIKI, T
    SAVONTAUS, ML
    ANVRET, M
    WILLIAMSON, R
    CYTOGENETICS AND CELL GENETICS, 1987, 46 (1-4): : 634 - 635
  • [28] PHYSICAL AND GENETIC-MAPPING OF THE MYOTONIC-DYSTROPHY LOCUS TO A 1-MB REGION ON CHROMOSOME-19
    HARLEY, HG
    CROW, SR
    RUNDLE, SA
    BROOK, JD
    JOHNSON, K
    HARPER, PS
    SHAW, DJ
    CYTOGENETICS AND CELL GENETICS, 1991, 58 (3-4): : 2019 - 2019
  • [29] LINKAGE DISEQUILIBRIUM DETECTED BETWEEN MYOTONIC-DYSTROPHY AND THE ANONYMOUS MARKER D19S63 IN THE SPANISH POPULATION
    COBO, A
    GRINBERG, D
    BALCELLS, S
    VILAGELIU, L
    GONZALEZDUARTE, R
    BAIGET, M
    HUMAN GENETICS, 1992, 89 (03) : 287 - 291
  • [30] 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, DAS
    HARPER, PS
    JOURNAL OF MEDICAL GENETICS, 1986, 23 (01) : 55 - 57