MENTAL-RETARDATION AND CONGENITAL-MALFORMATIONS ASSOCIATED WITH A RING CHROMOSOME 9

被引：23

作者：

NAKAJIMA, S

YANAGISAWA, M

KAMOSHITA, S

NAKAGOME, Y

机构：

[1] JICHI MED SCH,DEPT PEDIAT,TOCHIGI 32904,JAPAN

[2] NATL INST GENET,DEPT HUMAN GENET,SHIZUOKA,JAPAN

来源：

关键词：

D O I：

10.1007/BF00295818

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：289 / 293

页数：5

共 13 条

[1] ALFI O, 1973, ANN GENET-PARIS, V16, P17
[2] FRAISSE J, 1974, ANN GENET-PARIS, V17, P175
[3] FRIED K, 1975, CLIN GENET, V7, P192
[4] JACOBSEN P, 1973, CLIN GENET, V4, P434
[5] KISTENMACHER ML, 1970, AM J HUM GENET, V22, P304
[6] RING 13 CHROMOSOME IN A MALFORMED INFANT WITH SPECIAL REGARD TO BREAK POINT
KUROKI, Y
NAGANO, Y
[J]. PROCEEDINGS OF THE JAPAN ACADEMY, 1974, 50 (08): : 645 - 647
[7] MOORE TM, 1973, J MED GENET, V10, P299
[8] POINTS OF EXCHANGE IN A HUMAN NO 5 RING CHROMOSOME
NAKAGOME, Y
IINUMA, K
TANIGUCHI, K
[J]. CYTOGENETICS AND CELL GENETICS, 1973, 12 (01): : 35 - 39
[9] ONO K, 1974, JPN J HUM GENET, V19, P235
[10] VANDENBERGHE J, 1974, ANN GENET, V17, P29