PRENATAL-DIAGNOSIS OF CYSTIC KIDNEY-DISEASE WITH VENTRICULOMEGALY - A REPORT OF 6 CASES IN 2 RELATED SIBSHIPS

被引：8

作者：

REUSS, A

DENHOLLANDER, JC

NIERMEIJER, MF

WLADIMIROFF, JW

VANDIGGELEN, OP

LINDHOUT, D

LOS, FJ

机构：

[1] ERASMUS UNIV,DEPT OBSTET & GYNECOL,3000 DR ROTTERDAM,NETHERLANDS

[2] ERASMUS UNIV,DEPT PATHOL,3000 DR ROTTERDAM,NETHERLANDS

[3] ERASMUS UNIV,DEPT CLIN GENET,3000 DR ROTTERDAM,NETHERLANDS

来源：

AMERICAN JOURNAL OF MEDICAL GENETICS | 1989年 / 33卷 / 03期

关键词：

D O I：

10.1002/ajmg.1320330319

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：385 / 389

页数：5

共 16 条

[1] PREDICTIVE VALUE OF AMNIOTIC ACETYLCHOLINESTERASE ANALYSIS IN THE DIAGNOSIS OF FETAL-ABNORMALITY IN 3700 PREGNANCIES [J].

AITKEN, DA ;

MORRISON, NM ;

FERGUSONSMITH, MA .

PRENATAL DIAGNOSIS, 1984, 4 (05) :329-340

[2]

BROCK DJH, 1980, LANCET, V1, P773

[3] GEL-ELECTROPHORESIS OF AMNIOTIC-FLUID ACETYLCHOLINESTERASE AS AN AID TO THE PRENATAL DIAGNOSIS OF FETAL DEFECTS [J].

BROCK, DJH ;

HAYWARD, C .

CLINICA CHIMICA ACTA, 1980, 108 (01) :135-141

[4] PRENATAL-DIAGNOSIS OF NEURAL-TUBE DEFECTS - EXPERIENCES WITH ACETYLCHOLINESTERASE GEL-ELECTROPHORESIS [J].

CRANDALL, BF ;

KASHA, W ;

MATSUMOTO, M .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1982, 12 (03) :361-366

[5] ROUTINE AMNIOTIC-FLUID ALPHA-FETOPROTEIN ASSAY - EXPERIENCE WITH 40,000 PREGNANCIES [J].

CRANDALL, BF ;

MATSUMOTO, M .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 24 (01) :143-149

[6]

EDELMAN GM, 1984, ANNU REV NEUROSCI, V7, P339

[7] PSEUDO-ZELLWEGER SYNDROME - DEFICIENCIES IN SEVERAL PEROXISOMAL OXIDATIVE ACTIVITIES [J].

GOLDFISCHER, S ;

COLLINS, J ;

RAPIN, I ;

NEUMANN, P ;

NEGLIA, W ;

SPIRO, AJ ;

ISHII, T ;

ROELS, F ;

VAMECQ, J ;

VANHOOF, F .

JOURNAL OF PEDIATRICS, 1986, 108 (01) :25-32

[8] CONGENITAL NEPHROTIC SYNDROME [J].

HALLMAN, N ;

NORIO, R ;

RAPOLA, J .

NEPHRON, 1973, 11 (2-4) :101-110

[9] DEFECT OF CEREBELLAR PURKINJE-CELL HISTOGENESIS ASSOCIATED WITH TYPE-I AND TYPE-II RENAL CYSTIC-DISEASE [J].

KORNGUTH, S ;

KNOBELOCH, L ;

VISESKUL, C ;

GILBERT, E ;

OPITZ, J .

ACTA NEUROPATHOLOGICA, 1977, 40 (01) :1-9

[10] VARIABILITY IN THE SMITH-LEMLI-OPITZ SYNDROME - OVERLAP WITH THE MECKEL SYNDROME [J].

LOWRY, RB .

AMERICAN JOURNAL OF MEDICAL GENETICS, 1983, 14 (03) :429-433

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