STRUCTURAL ANOMALY (INV(P-Q+)) OF A C+X GROUP CHROMOSOME IN A DYSPLASTIC BOY WITH DISSOCIATED MENTAL DEVELOPMENT

被引:4
作者
KEUTEL, J
SCHUBERT, W
机构
[1] Institut für Humangenetik, Marburg
[2] Klinik für Kinder- und Jugendpsychiatrie der Universität, Marburg
来源
HUMANGENETIK | 1969年 / 7卷 / 02期
关键词
D O I
10.1007/BF00287076
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A boy with dissociation of mental development, slight diffuse encephalopathy, and few dysplasias is reported. Cytogenetic investigation of leukocytes and fibroblasts revealed a subtelocentric chromosome in group C+X whereas the caryotypes of the parents are normal. © 1969 Springer-Verlag.
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页码:119 / &
相关论文
共 6 条
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  • [2] DEGROUCHY J, 1967, ARCH FR PEDIATR, V24, P859
  • [3] JACOBS PA, 1967, ANN HUM GENET, V31, P219
  • [4] PITT DB, 1967, LANCET, V2, P568
  • [5] SCHILLING F, IN PRESS
  • [6] WONG J, 1966, HUMAN CHROMOSOME NEW, V19, P38