TURNER PHENOTYPE - MOSAIC 45,X/47,XY,+18

被引：23

作者：

SCHINZEL, A ^{[1
]}

SCHMID, W ^{[1
]}

PRADER, A ^{[1
]}

机构：

[1] UNIV ZURICH,DEPT PAEDIAT,DIV MED GENET,ZURICH,SWITZERLAND

来源：

关键词：

D O I：

10.1136/jmg.11.1.101

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：101 / 104

页数：4

共 13 条

[1] BERATIS NG, 1972, PEDIATRICS, V50, P908
[2] ANALYSIS OF HUMAN METAPHASE CHROMOSOME SET BY AID OF DNA-BINDING FLUORESCENT AGENTS
CASPERSSON, T
ZECH, L
JOHANSSON, C
[J]. EXPERIMENTAL CELL RESEARCH, 1970, 62 (2-3) : 490 - +
[3] DOUBLE ANEUPLOIDY (47,XX,21+/45,X) ARISING THROUGH SIMULTANEOUS DOUBLE NONDISJUNCTION
COHEN, MM
DAVIDSON, RG
[J]. JOURNAL OF MEDICAL GENETICS, 1972, 9 (02) : 242 - +
[4] EDGREN J, 1966, J MENT DEFIC RES, V10, P47
[5] HSU LYF, 1971, AM J HUM GENET, V23, P592
[6] SECONDARY NONDISJUNCTION CAUSING REGULAR TRISOMY 21 IN OFFSPRING OF A MOSAIC TRISOMY 21 MOTHER
KRMPOTIC, E
HARDIN, MB
[J]. AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1971, 110 (04) : 589 - &
[7] PFEIFFER RA, 1968, KARYOTYP PHANOTYP AU
[8] TURNERS SYNDROME IN ONE OF MONOZYGOTIC TWINS WITH MOSAICISM
POTTER, AM
TAITZ, LS
[J]. ACTA PAEDIATRICA SCANDINAVICA, 1972, 61 (04): : 473 - &
[9] PRIEUR M, 1972, ANN GENET-PARIS, V15, P195
[10] ROUBIN M, 1973, ANN GENET-PARIS, V16, P123