POSSIBLE COMPLEX TRANSLOCATION T(9-14-13) (Q12-P1 QUESTIONABLE-Q31) IN MOTHER OF A CHILD WITH 9P-TRISOMY SYNDROME

被引：41

作者：

FUJITA, H

ABE, T

YAMAMOTO, K

FURUYAMA, JI

机构：

[1] KYOTO PREFECTURAL UNIV MED,DEPT MED & PREVENT MED,KYOTO,JAPAN

[2] HYOGO COLL MED,DEPT GENET,HYOGO,JAPAN

[3] OSAKA CITY UNIV,FAC SCI LIVING,DEPT CHILD HLTH,OSAKA 459,SUMIYOSHI,JAPAN

来源：

HUMANGENETIK | 1974年 / 25卷 / 02期

关键词：

D O I：

10.1007/BF00283308

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：83 / 92

页数：10

共 17 条

[1] ABE T, 1969, JPN J HUM GENET, V14, P107
[2] FAMILIAL TRANSLOCATION INVOLVING CHROMOSOMES 6, 14 AND 20, IDENTIFIED BY QUINACRINE FLUORESCENCE
ALLDERDICE, PW
MILLER, OJ
MILLER, DA
BREG, WR
GENDEL, E
ZELSON, C
[J]. HUMANGENETIK, 1971, 13 (03): : 205 - +
[3] BLOOM GE, 1968, AM J HUM GENET, V20, P495
[4] BUTLER LJ, 1969, ANN GENET-PARIS, V12, P15
[5] CANTU JM, 1971, ANN GENET-PARIS, V14, P177
[6] CASPERSSON T, 1970, CHROMOSOMA, V30, P215
[7] CASE OF TRISOMY-9
FEINGOLD, M
ATKINS, L
[J]. JOURNAL OF MEDICAL GENETICS, 1973, 10 (02) : 184 - 187
[8] A COMPLEX FAMILIAL TRANSLOCATION INVOLVING CHROMOSOMES 5,9 AND 13
FREDGA, K
HALL, B
[J]. CYTOGENETICS, 1970, 9 (04): : 294 - &
[9] FUJITA H, 1971, JPN J HUM GENET, V15, P299
[10] SIBLINGS WITH DIFFERENT TYPES OF CHROMOSAL ABERRATIONS DUE TO D/E-TRANSLOCATION OF MOTHER
HAUSCHTE.E
MURSET, G
PRADER, A
BUHLER, E
[J]. CYTOGENETICS, 1966, 5 (05): : 281 - &