A GIRL WITH THE PRADER-WILLI SYNDROME AND ROBERTSONIAN TRANSLOCATION 45,XX,T(14-15)(P11-Q11) WHICH WAS PRESENT IN 3 NORMAL FAMILY MEMBERS

被引：48

作者：

SMITH, A ^{[1
]}

NOEL, M ^{[1
]}

机构：

[1] MED PRACTIT PENRTH,NSW,AUSTRALIA

来源：

关键词：

D O I：

10.1007/BF00291777

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：271 / 273

页数：3

共 24 条

[1] LOCALIZATION OF HETEROCHROMATIN IN HUMAN CHROMOSOMES [J].

ARRIGHI, FE ;

HSU, TC .

CYTOGENETICS, 1971, 10 (02) :81-&

[2]

CARREL RE, 1973, AM J MENT DEF, V77, P616

[3]

COHEN MM, 1971, ANN GENET-PARIS, V14, P87

[4]

DOYLE CT, 1976, HUM GENET, V33, P131

[5]

EMBERGER JM, 1977, ANN GENET-PARIS, V20, P297

[6]

ERDTMANN B, 1975, HUMANGENETIK, V26, P297

[7]

FAED MJW, 1979, CLIN GENET, V16, P191

[8] 15/15 TRANSLOCATION IN PRADER-WILLI SYNDROME [J].

FRACCARO, M ;

ZUFFARDI, O ;

BUHLER, EM ;

JURIK, LP .

[9]

FRACCARO M, 1979, KLINISCHE GENETIK PA

[10]

FUNDERBURK SJ, 1977, AM J HUM GENET, V29, P136