-transparent.png){kind=logo}
Parental origin of the extra haploid chromosome set in triploidies diagnosed prenatally. 1995
P Miny, and
B Koppers, and
B Dworniczak, and
N Bogdanova, and
W Holzgreve, and
S Tercanli, and
S Basaran, and
H Rehder, and
R Exeler, and
J Horst
Institute for Human Genetics, University of Münster, Germany.
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.
Related Publications
P Miny, and
B Koppers, and
B Dworniczak, and
N Bogdanova, and
W Holzgreve, and
S Tercanli, and
S Basaran, and
H Rehder, and
R Exeler, and
J Horst
March 2000,
Human genetics,
P Miny, and
B Koppers, and
B Dworniczak, and
N Bogdanova, and
W Holzgreve, and
S Tercanli, and
S Basaran, and
H Rehder, and
R Exeler, and
J Horst
March 1991,
American journal of medical genetics,
P Miny, and
B Koppers, and
B Dworniczak, and
N Bogdanova, and
W Holzgreve, and
S Tercanli, and
S Basaran, and
H Rehder, and
R Exeler, and
J Horst
February 2003,
Human reproduction (Oxford, England),
P Miny, and
B Koppers, and
B Dworniczak, and
N Bogdanova, and
W Holzgreve, and
S Tercanli, and
S Basaran, and
H Rehder, and
R Exeler, and
J Horst
October 1989,
American journal of human genetics,
P Miny, and
B Koppers, and
B Dworniczak, and
N Bogdanova, and
W Holzgreve, and
S Tercanli, and
S Basaran, and
H Rehder, and
R Exeler, and
J Horst
June 1977,
Human genetics,
P Miny, and
B Koppers, and
B Dworniczak, and
N Bogdanova, and
W Holzgreve, and
S Tercanli, and
S Basaran, and
H Rehder, and
R Exeler, and
J Horst
September 1982,
Journal of mental deficiency research,
P Miny, and
B Koppers, and
B Dworniczak, and
N Bogdanova, and
W Holzgreve, and
S Tercanli, and
S Basaran, and
H Rehder, and
R Exeler, and
J Horst
January 1996,
Annales de genetique,
P Miny, and
B Koppers, and
B Dworniczak, and
N Bogdanova, and
W Holzgreve, and
S Tercanli, and
S Basaran, and
H Rehder, and
R Exeler, and
J Horst
September 1995,
American journal of medical genetics,
P Miny, and
B Koppers, and
B Dworniczak, and
N Bogdanova, and
W Holzgreve, and
S Tercanli, and
S Basaran, and
H Rehder, and
R Exeler, and
J Horst
October 1983,
Tijdschrift voor kindergeneeskunde,
P Miny, and
B Koppers, and
B Dworniczak, and
N Bogdanova, and
W Holzgreve, and
S Tercanli, and
S Basaran, and
H Rehder, and
R Exeler, and
J Horst
August 1993,
Prenatal diagnosis,
