ROBERTS SYNDROME - CLINICAL AND CYTOGENETIC ASPECTS

被引：24

作者：

MANN, NP ^{[1
]}

FITZSIMMONS, J ^{[1
]}

FITZSIMMONS, E ^{[1
]}

COOKE, P ^{[1
]}

机构：

[1] CITY HOSP NOTTINGHAM,DEPT CLIN GENET,CLIN GENET SERV,NOTTINGHAM NG5 1PB,ENGLAND

来源：

关键词：

D O I：

10.1136/jmg.19.2.116

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：116 / 119

页数：4

共 8 条

[1]

FITZSIMMONS EM, 1980, NURS MIRROR, V5, P40

[2]

FREEMAN MVR, 1974, CLIN GENET, V5, P1

[3]

GERMAN J, 1979, CLIN GENET, V16, P441

[4] SC PHOCOMELIA AND ROBERTS SYNDROME - NOSOLOGIC ASPECTS [J].

HERRMANN, J ;

OPITZ, JM .

[5] FAMILIAL HOLOPROSENCEPHALY WITH ENDOCRINE DYSGENESIS [J].

HINTZ, RL ;

MENKING, M ;

SOTOS, JF .

JUDGE, C .

[7]

Roberts JB, 1919, ANN SURG, V70, P252

[8] ROBERTS SYNDROME AND CLONIDINE [J].

STOLL, C ;

LEVY, JM ;

BESHARA, D .