PARENTAL ORIGIN OF THE EXTRA HAPLOID CHROMOSOME SET IN TRIPLOIDIES DIAGNOSED PRENATALLY

被引:25
作者
MINY, P
KOPPERS, B
DWORNICZAK, B
BOGDANOVA, N
HOLZGREVE, W
TERCANLI, S
BASARAN, S
REHDER, H
EXELER, R
HORST, J
机构
[1] UNIV MUNSTER,CTR OBSTET & GYNECOL,D-48149 MUNSTER,GERMANY
[2] UNIV MARBURG,INST HUMAN GENET,W-3550 MARBURG,GERMANY
[3] UNIV ISTANBUL,DEPT PEDIAT,CAPA,TURKEY
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1995年 / 57卷 / 01期
关键词
TRIPLOIDY; IMPRINTING; POLYMORPHIC SATELLITES;
D O I
10.1002/ajmg.1320570121
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The parental origin of the additional chromosome complement in a total of 17 cases of triploidy was determined mainly using highly polymorphic microsatellites. Maternal origin of the triploidy was demonstrated in most cases. To the best of our knowledge, this is the first systematic evaluation of the parental origin of chromosome sets in fetuses who survived until a cytogenetic diagnosis was established. In contrast to previous investigations this study documented a predominance of maternal origin of the extra haploid set mainly due to longer survival time for digynic triploidies. The concept of 2 distinct fetal phenotypes in triploidy is clearly supported by this study. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:102 / 106
页数:5
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