TRISOMY 9 ASSOCIATED WITH AN ENLARGED 9QH SEGMENT IN A LIVEBORN

被引:39
作者
SEABRIGHT, M [1 ]
GREGSON, N [1 ]
MOULD, S [1 ]
机构
[1] GEN HOSP,WESSEX REG CYTOGENET,SALISBURY,WILTSHIRE,ENGLAND
关键词
D O I
10.1007/BF00295299
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:323 / 325
页数:3
相关论文
共 8 条
[1]   CASE OF TRISOMY-9 [J].
FEINGOLD, M ;
ATKINS, L .
JOURNAL OF MEDICAL GENETICS, 1973, 10 (02) :184-187
[2]   PRENATAL DIAGNOSIS OF TRISOMY 9 [J].
FRANCKE, U ;
BENIRSCHKE, K ;
JONES, OW .
HUMANGENETIK, 1975, 29 (03) :243-250
[3]  
KAJII T, 1973, AM J HUM GENET, V25, P539
[4]   FREQUENCY OF 9QH+ AND RISK OF CHROMOSOME-ABERRATIONS IN PROGENY OF INDIVIDUALS WITH 9QH+ [J].
NIELSEN, J ;
FRIEDRICH, U ;
HREIDARSSON, AB ;
ZEUTHEN, E .
HUMANGENETIK, 1974, 21 (03) :211-216
[5]  
SEABRIGH.M, 1971, LANCET, V2, P971
[6]   SIMPLE TECHNIQUE FOR DEMONSTRATING CENTROMERIC HETEROCHROMATIN [J].
SUMNER, AT .
EXPERIMENTAL CELL RESEARCH, 1972, 75 (01) :304-&
[7]   PARTIAL AND COMPLETE TRISOMY-9 - DELINEATION OF A TRISOMY-9 SYNDROME [J].
SUTHERLAND, GR ;
CARTER, RF ;
MORRIS, LL .
HUMAN GENETICS, 1976, 32 (02) :133-140
[8]  
1975, BIRTH DEFECTS OAS