LINKAGE OF AUTOSOMAL DOMINANT MYOTONIA-CONGENITA (THOMSEN DISEASE) TO THE TCRB GENE LOCUS ON CHROMOSOME-7Q35

被引:0
|
作者
ABDALLA, JA
CASLEY, WL
COUSIN, HK
HASHIMOTO, L
ARMSTRONG, HA
HUDSON, AJ
EBERS, GC
MURPHY, EG
CORNELIS, FC
机构
关键词
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
引用
收藏
页码:1426 / 1426
页数:1
相关论文
共 50 条
  • [41] REFINING THE LOCALIZATION OF THE PKD2 LOCUS ON CHROMOSOME 4Q BY LINKAGE ANALYSIS IN SPANISH FAMILIES WITH AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE TYPE-2
    SANMILLAN, JL
    VIRIBAY, M
    PERAL, B
    MARTINEZ, I
    WEISSENBACH, J
    MORENO, F
    AMERICAN JOURNAL OF HUMAN GENETICS, 1995, 56 (01) : 248 - 253
  • [42] EVIDENCE FOR A MAJOR GENE (RP10) FOR AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA ON CHROMOSOME-7Q - LINKAGE MANNING IN A 2ND, UNRELATED FAMILY
    MCGUIRE, RE
    GANNON, AM
    SULLIVAN, LS
    RODRIGUEZ, JA
    DAIGER, SP
    HUMAN GENETICS, 1995, 95 (01) : 71 - 74
  • [43] IDENTIFICATION OF A LOCUS WHICH SHOWS NO GENETIC-RECOMBINATION WITH THE AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY-DISEASE GENE ON CHROMOSOME-16
    GERMINO, GG
    BARTON, NJ
    LAMB, J
    HIGGS, DR
    HARRIS, P
    XIAO, GH
    SCHERER, G
    NAKAMURA, Y
    REEDERS, ST
    AMERICAN JOURNAL OF HUMAN GENETICS, 1990, 46 (05) : 925 - 933
  • [44] AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPLEGIA - REDUCTION OF THE FSPI CANDIDATE REGION ON CHROMOSOME 14Q TO 7-CM AND LOCUS HETEROGENEITY
    GISPERT, S
    SANTOS, N
    DAMEN, R
    VOIT, T
    SCHULZ, J
    KLOCKGETHER, T
    OROZCO, G
    KREUZ, F
    WEISSENBACH, J
    AUBURGER, G
    AMERICAN JOURNAL OF HUMAN GENETICS, 1995, 56 (01) : 183 - 187
  • [45] Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34 (vol 62, pg 633, 1998)
    Chance, PF
    Rabin, BA
    Ryan, SG
    Ding, Y
    Scavina, M
    Conway, D
    Crain, B
    Griffin, JW
    Cornblath, DR
    AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (01) : 295 - 295
  • [46] AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE - LOCALIZATION OF THE 2ND GENE TO CHROMOSOME-4Q13-Q23
    KIMBERLING, WJ
    KUMAR, S
    GABOW, PA
    KENYON, JB
    CONNOLLY, CJ
    SOMLO, S
    GENOMICS, 1993, 18 (03) : 467 - 472
  • [47] AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE DOES NOT MAP TO THE 2ND GENE LOCUS FOR AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE ON CHROMOSOME-4
    ZERRES, K
    MUCHER, G
    RUDNIKSCHONEBORN, S
    HUMAN GENETICS, 1994, 93 (06) : 697 - 698
  • [48] A SEGMENT FROM THE CHROMOSOME 16 AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY-DISEASE LOCUS (ADPKD) IS HOMOLOGOUS TO MEMBERS OF A MULTI-GENE FAMILY
    SOMLO, S
    GILLESPIE, GAJ
    WEINSTAT, DL
    GERMINO, GG
    REEDERS, ST
    KIDNEY INTERNATIONAL, 1990, 37 (01) : 521 - 521
  • [49] Autosomal-dominant, prelingual, nonprogressive sensorineural hearing loss: localization of the gene (DFNA8) to chromosome 11q by linkage in an Austrian family
    Kirschhofer, K
    Kenyon, JB
    Hoover, DM
    Franz, P
    Weipoltshammer, K
    Wachtler, F
    Kimberling, WJ
    CYTOGENETICS AND CELL GENETICS, 1998, 82 (1-2): : 126 - 130
  • [50] A new gene locus for an autosomal-dominant non-syndromic hearing impairment (DFNA 33) is situated on chromosome 13q34-qter
    Boensch, D.
    Schmidt, C. -M.
    Scheer, P.
    Bohlender, J.
    Neumann, C.
    Zehnhoff-Dinnesen, A. Am
    Deufel, T.
    HNO, 2009, 57 (04) : 371 - 376