G-DELETION SYNDROMES

被引：64
作者：
WARREN, RJ
RIMOIN, DL
机构：
来源：
JOURNAL OF PEDIATRICS | 1970年 / 77卷 / 04期
关键词：
D O I：
10.1016/S0022-3476(70)80209-8
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
引用
收藏
页码：658 / +
页数：1
相关论文
共 30 条
  • [1] AUTOSOMAL MONOSOMY IN MAN - COMPLETE MONOSOMY G (21-22) IN A 4-AND-1/2-YEAR-OLD MENTALLY RETARDED GIRL
    ALAISH, MS
    DELACRUZ, F
    GOLDSMITH, LA
    VOLPE, J
    MELLA, G
    ROBINSON, JC
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1967, 277 (15) : 777 - +
  • [2] ALLDERDICE PW, 1969, AM J HUM GENET, V21, P499
  • [3] BAUCHINGER M, 1968, HUMANGENETIK, V6, P303
  • [4] BLANK C E, 1969, Journal of Medical Genetics, V6, P220, DOI 10.1136/jmg.6.2.220
  • [5] Broyer M, 1966, Presse Med, V74, P791
  • [6] MONOSOMY FOR A G AUTOSOME
    CHALLACOMBE, DN
    TAYLOR, A
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1969, 44 (233) : 113 - +
  • [7] PYCNODYSOSTOSIS WITH A FAMILIAL CHROMOSOME ANOMALY
    ELMORE, SM
    NANCE, WE
    MCGEE, BJ
    ENGELDEM.M
    ENGEL, E
    [J]. AMERICAN JOURNAL OF MEDICINE, 1966, 40 (02) : 273 - &
  • [8] ANTIMONGOLISM SYNDROME
    ENDO, A
    YAMAMOTO, M
    SUZUKI, Y
    SAKAI, K
    [J]. BRITISH MEDICAL JOURNAL, 1969, 4 (5676) : 148 - &
  • [9] ENGEL E, 1966, LANCET, V1, P1130
  • [10] A RING D CHROMOSOME AND ANOMALOUS INHERITANCE OF HAPTOGLOBIN TYPE
    GERALD, PS
    WARNER, S
    SINGER, JD
    CORCORAN, PA
    UMANSKY, I
    [J]. JOURNAL OF PEDIATRICS, 1967, 70 (02) : 172 - +
123