PRENATAL-DIAGNOSIS OF A PROBABLE HEREDITARY SYNDROME WITH HOLOPROSENCEPHALY, HYDROCEPHALY, OCTODACTYLY, AND CARDIAC-MALFORMATIONS

被引：13

作者：

GROTE, W

REHDER, H

WEISNER, D

WIEDEMANN, HR

机构：

[1] UNIV KIEL,DEPT GYNAECOL & OBSTET,D-2300 KIEL 1,FED REP GER

[2] UNIV KIEL,DEPT PHARM,D-2300 KIEL 1,FED REP GER

[3] UNIV LUBECK,DEPT HUMAN GENET,LUBECK,FED REP GER

来源：

关键词：

D O I：

10.1007/BF00445808

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：155 / 157

页数：3

共 6 条

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[2] PRENATAL MORPHOLOGY IN MECKELS SYNDROME
REHDER, H
LABBE, F
[J]. PRENATAL DIAGNOSIS, 1981, 1 (03) : 161 - 172
[3] SALONEN R, 1981, CLIN GENET, V19, P321
[4] SMITH DW, 1982, RECOGNIZABLE PATTERN, P140
[5] HEPTACARPO-OCTATARSO-DACTYLY COMBINED WITH MULTIPLE MALFORMATIONS
TOLLNER, U
HORST, J
MANZKE, L
SCHMID, M
NESTLERWOCHER, H
WECKLER, C
[J]. EUROPEAN JOURNAL OF PEDIATRICS, 1981, 136 (02) : 207 - 210
[6] WITKOWSKI R, 1983, GENETIK ERBLICHER SY, P567