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Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres.
Published in:
European Journal of Human Genetics, 2012, v. 20, n. 9, p. 1010, doi. 10.1038/ejhg.2012.122
By:
- Van Rij, Maartje C;
- De Rademaeker, Marjan;
- Moutou, Céline;
- Dreesen, Jos C F M;
- De Rycke, Martine;
- Liebaers, Inge;
- Geraedts, Joep P M;
- De Die-Smulders, Christine E M;
- Viville, Stéphane
Publication type:
Article
Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres.
Published in:
European Journal of Human Genetics, 2012, v. 20, n. 4, p. 368, doi. 10.1038/ejhg.2011.202
By:
- Van Rij, Maartje C;
- De Rademaeker, Marjan;
- Moutou, Céline;
- Dreesen, Jos CFM;
- De Rycke, Martine;
- Liebaers, Inge;
- Geraedts, Joep PM;
- De Die-Smulders, Christine EM;
- Viville, Stéphane
Publication type:
Article
Preimplantation genetic diagnosis for myotonic dystrophy type 1: upon request to child.
Published in:
European Journal of Human Genetics, 2009, v. 17, n. 11, p. 1403, doi. 10.1038/ejhg.2009.56
By:
- De Rademaeker, Marjan;
- Verpoest, Willem;
- De Rycke, Martine;
- Seneca, Sara;
- Sermon, Karen;
- Desmyttere, Sonja;
- Bonduelle, Maryse;
- Van der Elst, Josianne;
- Devroey, Paul;
- Liebaers, Inge
Publication type:
Article
Risk of malignancy in 22q11.2 deletion syndrome.
Published in:
Clinical Case Reports, 2017, v. 5, n. 4, p. 486, doi. 10.1002/ccr3.880
By:
- Stevens, Toer;
- Werff ten Bosch, Jutte;
- De Rademaeker, Marjan;
- Van Den Bogaert, Ann;
- Akker, Machiel
Publication type:
Article
The reproductive outcome of female patients with myotonic dystrophy type 1 (DM1) undergoing PGD is not affected by the size of the expanded CTG repeat tract.
Published in:
Journal of Assisted Reproduction & Genetics, 2010, v. 27, n. 6, p. 327, doi. 10.1007/s10815-010-9392-9
By:
- Verpoest, Willem;
- Seneca, Sara;
- De Rademaeker, Marjan;
- Sermon, Karen;
- De Rycke, Martine;
- De Vos, Michel;
- Haentjens, Patrick;
- Devroey, Paul;
- Liebaers, Ingeborg
Publication type:
Article
Implementation of Exome Sequencing in Prenatal Diagnostics: Chances and Challenges.
Published in:
Diagnostics (2075-4418), 2023, v. 13, n. 5, p. 860, doi. 10.3390/diagnostics13050860
By:
- Janicki, Ewa;
- De Rademaeker, Marjan;
- Meunier, Colombine;
- Boeckx, Nele;
- Blaumeiser, Bettina;
- Janssens, Katrien
Publication type:
Article
Prenatally detected copy number variants in a national cohort: A postnatal follow‐up study.
Published in:
Prenatal Diagnosis, 2020, v. 40, n. 10, p. 1272, doi. 10.1002/pd.5751
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
Publication type:
Article
The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations.
Published in:
2018
By:
- Muys, Joke;
- Blaumeiser, Bettina;
- Jacquemyn, Yves;
- Bandelier, Claude;
- Brison, Nathalie;
- Bulk, Saskia;
- Chiarappa, Patrizia;
- Courtens, Winnie;
- De Leener, Anne;
- De Rademaeker, Marjan;
- Désir, Julie;
- Destrée, Anne;
- Devriendt, Koenraad;
- Dheedene, Annelies;
- Fieuw, Annelies;
- Fransen, Erik;
- Gatot, Jean‐Stéphane;
- Holmgren, Philip;
- Jamar, Mauricette;
- Janssens, Sandra
Publication type:
journal article
An Augmented ABCA4 Screen Targeting Noncoding Regions Reveals a Deep Intronic Founder Variant in Belgian Stargardt Patients.
Published in:
Human Mutation, 2015, v. 36, n. 1, p. 39, doi. 10.1002/humu.22716
By:
- Bauwens, Miriam;
- De Zaeytijd, Julie;
- Weisschuh, Nicole;
- Kohl, Susanne;
- Meire, Françoise;
- Dahan, Karin;
- Depasse, Fanny;
- De Jaegere, Sarah;
- De Ravel, Thomy;
- De Rademaeker, Marjan;
- Loeys, Bart;
- Coppieters, Frauke;
- Leroy, Bart P.;
- De Baere, Elfride
Publication type:
Article
Subtelomeric imbalances in phenotypically normal individuals.
Published in:
Human Mutation, 2007, v. 28, n. 10, p. 958, doi. 10.1002/humu.20537
By:
- Balikova, Irina;
- Menten, Björn;
- de Ravel, Thomy;
- Le Caignec, Cédric;
- Thienpont, Bernard;
- Urbina, Montse;
- Doco-Fenzy, Martine;
- de Rademaeker, Marjan;
- Mortier, Geert;
- Kooy, Frank;
- van Den Ende, Janneke;
- Devriendt, Koen;
- Fryns, Jean-Pierre;
- Speleman, Frank;
- Vermeesch, Joris Robert
Publication type:
Article

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