A new rapid test (fluorescence in situ hybridisation [FISH]) in the prenatal diagnosis of the most common chromosomal aberrations: what is their practical value?

被引：3

作者：

Eiben, B

Hammans, W

Goebel, R

Epplen, JT

机构：

[1] Evangel Krankenhaus, Inst Klin Genet, D-46067 Oberhausen, Germany

[2] Evangel Krankenhaus, Frauenklin, D-46067 Oberhausen, Germany

[3] Ruhr Univ Bochum, Abt Mol Humangenet, D-44780 Bochum, Germany

来源：

DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT | 1998年 / 123卷 / 03期

关键词：

D O I：

10.1055/s-2007-1023898

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：55 / 57

页数：3

共 8 条

[1]

BRYNDORF T, 1997, PRENAT DIAGN, V17, P331

[2]

Eiben B, 1996, LANCET, V347, P1553

[3] On the complication risk of early amniocentesis versus standard amniocentesis [J].

Eiben, B ;

Hammans, W ;

Hansen, S ;

Trawicki, W ;

Osthelder, B ;

Stelzer, A ;

Jaspers, KD ;

Goebel, R .

FETAL DIAGNOSIS AND THERAPY, 1997, 12 (03) :140-144

[4]

EIBEN B, 1997, IN PRESS PRENAT DIAG

[5]

Fritz B, 1996, Z GEBURTSH NEONATOL, V200, P191

[6]

KLINGER K, 1992, AM J HUM GENET, V51, P55

[7] CROSS-HYBRIDIZATION OF THE CHROMOSOME-13/21 ALPHA-SATELLITE DNA-PROBE TO CHROMOSOME-22 IN THE PRENATAL SCREENING OF COMMON CHROMOSOMAL ANEUPLOIDIES BY FISH [J].

VERLINSKY, Y ;

GINSBERG, N ;

CHMURA, M ;

FREIDINE, M ;

WHITE, M ;

STROM, C ;

KULIEV, A .

PRENATAL DIAGNOSIS, 1995, 15 (09) :831-834

[8]

WARD BE, 1993, AM J HUM GENET, V52, P854

← 1 →