Search Results - "Dheedene, A"

Chromosomal mosaicism in human blastocysts: the ultimate challenge of preimplantation genetic testing? by Popovic, M, Dheedene, A, Christodoulou, C, Taelman, J, Dhaenens, L, Van Nieuwerburgh, F, Deforce, D, Van den Abbeel, E, De Sutter, P, Menten, B, Heindryckx, B

“…Abstract STUDY QUESTION To what extent does a trophectoderm (TE) biopsy reliably reflect the chromosomal constitution of the inner cell mass (ICM) in human…”
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Extended in vitro culture of human embryos demonstrates the complex nature of diagnosing chromosomal mosaicism from a single trophectoderm biopsy by Popovic, M, Dhaenens, L, Taelman, J, Dheedene, A, Bialecka, M, De Sutter, P, Chuva de Sousa Lopes, S M, Menten, B, Heindryckx, B

“…Abstract STUDY QUESTION What is the accuracy of preimplantation genetic testing for aneuploidies (PGT-A) when considering human peri-implantation outcomes in…”
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GENType: all-in-one preimplantation genetic testing by pedigree haplotyping and copy number profiling suitable for third-party reproduction by De Witte, L, Raman, L, Baetens, M, De Koker, A, Callewaert, N, Symoens, S, Tilleman, K, Vanden Meerschaut, F, Dheedene, A, Menten, B

“…Abstract STUDY QUESTION Is it possible to develop a comprehensive pipeline for all-in-one preimplantation genetic testing (PGT), also suitable for parents-only…”
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Extended In Vitro Culture of Human Embryos Demonstrates the Complex Nature of Diagnosing Chromosomal Mosaicism From a Single Trophectoderm Biopsy by Popovic, M, Dhaenens, L, Taelman, J, Dheedene, A, Bialecka, M, De Sutter, P, de Sousa Lopes, S. M Chuva, Menten, B, Heindryckx, B

“…(Abstracted from Hum Reprod 2019;34(4):758–769)The development of preimplantation genetic testing (PGT-A) in conjunction with assisted reproductive technology…”
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A de novo POU3F3 Deletion in a Boy with Intellectual Disability and Dysmorphic Features by Dheedene, A., Maes, M., Vergult, S., Menten, B.

“…We describe a boy presenting with intellectual disability and dysmorphic features in whom a cryptic microdeletion in chromosome band 2q12.1 was identified with…”
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Prenatally detected copy number variants in a national cohort: A postnatal follow‐up study by Muys, Joke, Jacquemyn, Yves, Blaumeiser, Bettina, Bourlard, Laura, Brison, Nathalie, Bulk, Saskia, Chiarappa, Patrizia, De Leener, Anne, De Rademaeker, Marjan, Désir, Julie, Destrée, Anne, Devriendt, Koenraad, Dheedene, Annelies, Duquenne, Armelle, Fieuw, Annelies, Fransen, Erik, Gatot, Jean‐Stéphane, Jamar, Mauricette, Janssens, Sandra, Kerstjens, Jorien, Keymolen, Kathelijn, Lederer, Damien, Menten, Björn, Pichon, Bruno, Rombout, Sonia, Sznajer, Yves, Van Den Bogaert, Ann, Van Den Bogaert, Kris, Vermeesch, Joris, Janssens, Katrien

“…Objective Belgian genetic centers established a database containing data on all chromosomal microarrays performed in a prenatal context. A study was initiated…”
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A de novo POU3F3 Deletion in a Boy with Intellectual Disability and Dysmorphic Features by Dheedene, A, Maes, M, Vergult, S, Menten, B

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