Zobrazeno 1 - 10
of 150
pro vyhledávání: '"Joy D. A. Delhanty"'
Autor:
Joy D. A. Delhanty
Publikováno v:
eLS
At birth, at least 1% of humans have a clinically significant chromosomal abnormality. However, this represents a small fraction of those originally conceived since by the time of birth, natural selection has eliminated the vast majority of abnormal
Autor:
Joris Vermeesch, Carlos Simón, Alan H. Handyside, Antonio Capalbo, Edith Coonen, Jamie Grifo, Rita Vassena, Joyce C. Harper, David R. Meldrum, Nathan R. Treff, Joy D. A. Delhanty, Carmen Rubio, Richard T. Scott, Jacques Cohen, Markus Montag, G Kokkali, Karen Sermon, Joep P.M. Geraedts, Martine De Rycke, Francesco Fiorentino, Laura Rienzi, Anick De Vos, Sebastiaan Mastenbroek, Marcos Meseguer, Filippo Maria Ubaldi, Dagan Wells, Santiago Munné, Norbert Gleicher, Jason E. Swain, K. Scott, Georg Griesinger, Willem Verpoest
Publikováno v:
Molecular Human Reproduction, 22(8), 545-557. Oxford University Press
MOLECULAR HUMAN REPRODUCTION
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname
MOLECULAR HUMAN REPRODUCTION
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname
STUDY QUESTION: We wanted to probe the opinions and current practices on preimplantation genetic screening (PGS), and more specifically on PGS in its newest form: PGS 2.0? STUDY FINDING: Consensus is lacking on which patient groups, if any at all, ca
Publikováno v:
Journal of Assisted Reproduction and Genetics. 36:2419-2419
The original article unfortunately contained a mistake. In the online version of the paper, the words "MII (metaphase II)-PB1 (1st polar body) complex (MII-PB1 complex)" in table 1 are incorrectly placed.
Publikováno v:
Reproductive BioMedicine Online. 28:624-637
This is a retrospective study aiming to assess telomere length in human embryos 4 days post fertilization and to determine whether it is correlated to chromosomal ploidy, embryo developmental rate and patient age. Embryos were donated from patients u
Autor:
Sioban SenGupta, Paul Serhal, Susannah Sargeant, H. Ghevaria, Urvashi Sarna, Joy D. A. Delhanty
Publikováno v:
Cytogenetic and Genome Research. 144:264-274
Germinal mosaicism in a parent is considered to be a rare cause of aneuploidy in the offspring. The aim of this study was to assess the incidence of pre-meiotic errors, indicative of germinal mosaicism, leading to aneuploidy compared with those that
Autor:
Sioban SenGupta, Joy D. A. Delhanty
Publikováno v:
Expert Review of Molecular Diagnostics. 12:585-592
Over the last 20 years, preimplantation genetic diagnosis (PGD) has changed from being an experimental procedure to one that is carried out in specialized diagnostic centers worldwide. Genetic awareness and the rapid identification of germline mutati
Publikováno v:
Cytogenetic and Genome Research. 136:21-29
Chromosome breakage is a fairly widespread phenomenon in preimplantation embryos affecting at least 10% of day 3 cleavage stage embryos. It may be detected during preimplantation genetic diagnosis (PGD). For carriers of structural chromosomal abnorma
Autor:
M. De Braekeleer, K.G.L. Fonseka, T. Voet, M. Yerle, D. Wells, A. Kanesky, J. Navarro, L. Ramos, J. Riquet, J.L. Barbero, A. Estop, M. Regev, D.K. Griffin, Satz Mengensatzproduktion, F. Morel, N. Mary, U. Eichenlaub-Ritter, F. Vidal, A.L. Marston, O. Reish, A. Pinton, Franck Pellestor, V. Amice, M.-J. Le Bris, M. Bordedebat, C. Templado, I. Matos, A. Mantzouratou, S. Girafi, A. Basinko, F. Pacchierotti, I. Lebedev, H. Barasc, J. Selva, N. Gueganic, I. Raymond Letron, F. Vialard, J.R. Vermeesch, N. Douet-Guilbert, N. Bonnet, D. Gisselsson, E. Fragouli, A. Ducos, A. Calgaro, Druck Reinhardt Druck Basel, Joy D. A. Delhanty, J.D.A. Delhanty, K. Feve, A.M. Dudez, M. Mashevich, H. Homer, A. Obradors, D. Molina-Gomes, F. Boitrelle, G. Daina, H. Maiato, K. Massip, A. Perrin, J. Benet, D. Clift, E. Vanneste, M. Rius, D. Ioannou
Publikováno v:
Cytogenetic and Genome Research. 133:I-IV
Autor:
Joy D. A. Delhanty
Publikováno v:
Cytogenetic and Genome Research. 133:136-140
Germline mosaicism has been thought to be a rare cause of aneuploidy in the human population. Recent evidence from cytological and population studies suggests otherwise. Approximately 5% of young couples with a Down syndrome child show evidence of ge
Publikováno v:
Fertility and Sterility. 94:1674-1679
Objective To overcome problems associated with the use of triplet repeat primed polymerase chain reaction (TP-PCR) in preimplantation genetic diagnosis (PGD) of myotonic dystrophy type 1 (DM1). Design Clinical research study. Setting UCL Centre for P