PRADER-WILLI SYNDROME AND CHROMOSOME-15 - A CLINICAL DISCUSSION OF 20 CASES

被引:67
作者
MATTEI, JF [1 ]
MATTEI, MG [1 ]
GIRAUD, F [1 ]
机构
[1] HOP ENFANTS TIMONE,CTR GENET MED,F-13385 MARSEILLE 5,FRANCE
关键词
D O I
10.1007/BF00292367
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:356 / 362
页数:7
相关论文
共 32 条
  • [1] SYSTEMATIC ANALYSIS OF 95 RECIPROCAL TRANSLOCATIONS OF AUTOSOMES
    AURIAS, A
    PRIEUR, M
    DUTRILLAUX, B
    LEJEUNE, J
    [J]. HUMAN GENETICS, 1978, 45 (03) : 259 - 282
  • [2] ABNORMAL CHILDHOOD PHENOTYPES ASSOCIATED WITH THE SAME BALANCED CHROMOSOME REARRANGEMENTS AS IN THE PARENTS
    AYME, S
    MATTEI, MG
    MATTEI, JF
    GIRAUD, F
    [J]. HUMAN GENETICS, 1979, 48 (01) : 7 - 12
  • [3] BALESTRAZZI P, 1983, HUM GENET
  • [4] CAVALLI J, 1982, HUM HERED, V32, P149
  • [5] PRADER-WILLI SYNDROME - VARIABLE SEVERITY AND RECURRENCE RISK
    CLARREN, SK
    SMITH, DW
    [J]. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1977, 131 (07): : 798 - 800
  • [6] FLEISCHNICK E, 1979, AM J HUM GENET, V31, pA94
  • [7] 15/15 TRANSLOCATION IN PRADER-WILLI SYNDROME
    FRACCARO, M
    ZUFFARDI, O
    BUHLER, EM
    JURIK, LP
    [J]. JOURNAL OF MEDICAL GENETICS, 1977, 14 (04) : 275 - 276
  • [8] AN EXTRA IDIC(15P)(Q11) CHROMOSOME IN PRADER-WILLI SYNDROME
    FUJITA, H
    SAKAMOTO, Y
    HAMAMOTO, Y
    [J]. HUMAN GENETICS, 1980, 55 (03) : 409 - 411
  • [9] FUNDERBURK SJ, 1977, AM J HUM GENET, V29, P136
  • [10] GABILAN JC, 1968, ARCH FR PEDIATR, V25, P121