Triploidy Detection
Triploidy Detection is a cytogenetic screening methodology within prenatal genetic diagnosis that identifies fetal triploidy by distinguishing the presence of a complete extra set of chromosomes from other aneuploidies through molecular karyotyping or quantitative fluorescent polymerase chain reaction.
106
Publications
4.4K
Citations
498
Authors
180
Institutions
Publications per year
2017–2026
10
106
1–5 of 106
498
Harris Birthright Research Centre for Fetal Medicine, United Kingdom
5 publications · 606 citations
5
h-index
3
h-index
3
h-index
Guy's and St Thomas' NHS Foundation Trust, United Kingdom
3 publications · 206 citations
3
h-index
Guy's and St Thomas' NHS Foundation Trust, United Kingdom
3 publications · 206 citations
3
h-index
1–5 of 498
180
University College London
London, United Kingdom
6 h-index
22 publications
950 citations
Harris Birthright Research Centre for Fetal Medicine
London, United Kingdom
5 h-index
19 publications
2.2K citations
King's College Hospital
London, United Kingdom
4 h-index
18 publications
2.1K citations
Japan Fisheries Research and Education Agency
Yokohama, Japan
3 h-index
6 publications
266 citations
Centre Hospitalier Intercommunal de Poissy
Saint-Germain-en-Laye, France
2 h-index
9 publications
606 citations
Ehime University
Matsuyama, Japan
2 h-index
2 publications
95 citations
Framingham State University
Framingham, United States
2 h-index
4 publications
110 citations
Baylor College of Medicine
Houston, United States
2 h-index
3 publications
152 citations
1–8 of 180
24 publications · 1.4K citations
19
h-index
10 publications · 469 citations
10
h-index
AJOG · 6 publications · 457 citations
6
h-index
Repository · 4 publications · 58 citations
4
h-index
3 publications · 75 citations
3
h-index
1–5