REPORT OF THE COMMITTEE ON CLINICAL DISORDERS, CHROMOSOME-ABERRATIONS AND UNIPARENTAL DISOMY

被引:61
作者
FREZAL, J [1 ]
SCHINZEL, A [1 ]
机构
[1] INST MED GENET, CH-8001 ZURICH, SWITZERLAND
来源
CYTOGENETICS AND CELL GENETICS | 1991年 / 58卷 / 3-4期
关键词
D O I
10.1159/000133716
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
引用
收藏
页码:986 / 1052
页数:67
相关论文
共 548 条
  • [1] ALITALO T, 1991, AM J HUM GENET, V48, P31
  • [2] ALAGILLE SYNDROME AND DELETION OF 20P
    ANAD, F
    BURN, J
    MATTHEWS, D
    CROSS, I
    DAVISON, BCC
    MUELLER, R
    SANDS, M
    LILLINGTON, DM
    EASTHAM, E
    [J]. JOURNAL OF MEDICAL GENETICS, 1990, 27 (12) : 729 - 737
  • [3] [Anonymous], AM J MED GENET
  • [4] ANVRET M, 1991, HUM GENET, V86, P481
  • [5] ARCHIDIACONO N, 1991, HUM GENET, V86, P604
  • [6] ARIAS S, 1989, CYTOGENET CELL GENET, V51, P953
  • [7] RECOMBINATIONS BETWEEN ALU REPEAT SEQUENCES THAT RESULT IN PARTIAL DELETIONS WITHIN THE C1-INHIBITOR GENE
    ARIGA, T
    CARTER, PE
    DAVIS, AE
    [J]. GENOMICS, 1990, 8 (04) : 607 - 613
  • [8] MUTATION OF THE SIGNAL PEPTIDE-ENCODING REGION OF THE PREPROPARATHYROID HORMONE GENE IN FAMILIAL ISOLATED HYPOPARATHYROIDISM
    ARNOLD, A
    HORST, SA
    GARDELLA, TJ
    BABA, H
    LEVINE, MA
    KRONENBERG, HM
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (04) : 1084 - 1087
  • [9] ARVEILER B, 1990, AM J HUM GENET, V46, P906
  • [10] LINKAGE ANALYSIS SUGGESTS AT LEAST 2 LOCI FOR X-LINKED NON-SPECIFIC MENTAL-RETARDATION
    ARVEILER, B
    ALEMBIK, Y
    HANAUER, A
    JACOBS, P
    TRANEBJAERG, L
    MIKKELSEN, M
    PUISSANT, H
    PIET, LL
    MANDEL, JL
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1988, 30 (1-2): : 473 - 483