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Marjan De Rademaeker

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Journal of Perinatal Medicine|October 27, 2025
Diagnostic yield and clinical impact of prenatal whole exome sequencing (WES) - four-year single center experienceKatleen Janssens, Marjan De Rademaeker, Joke Muys, et al.
Diagnostics (Basel, Switzerland)|March 11, 2023
Implementation of Exome Sequencing in Prenatal Diagnostics: Chances and ChallengesEwa Janicki, Marjan De Rademaeker, Colombine Meunier, et al.
Clinical Genetics|October 22, 2024
RNU4-2-Related Neurodevelopmental Disorder Is Associated With a Recognisable Facial GestaltJessica Rosenblum, Diane Beysen, Anna C Jansen, et al.
Clinical Case Reports|April 12, 2017
Risk of malignancy in 22q11.2 deletion syndromeToer Stevens, Jutte van der Werff Ten Bosch, Marjan De Rademaeker, et al.
European Journal of Medical Genetics|March 8, 2025
Paracentric inversion disrupting the SHANK2 geneJolien Huyghebaert, Bregje Christiaenssen, Marjan De Rademaeker, et al.
Journal of Assisted Reproduction and Genetics|March 12, 2010
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 tractWillem Verpoest, Sara Seneca, Marjan De Rademaeker, et al.
European Journal of Human Genetics : EJHG|April 16, 2009
Preimplantation genetic diagnosis for myotonic dystrophy type 1: upon request to childMarjan De Rademaeker, Willem Verpoest, Martine De Rycke, et al.
The Journal of Molecular Diagnostics : JMD|August 28, 2012
Reliable and sensitive detection of fragile X (expanded) alleles in clinical prenatal DNA samples with a fast turnaround timeSara Seneca, Willy Lissens, Kristof Endels, et al.
European Journal of Human Genetics : EJHG|November 11, 2011
Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centresMaartje C Van Rij, Marjan De Rademaeker, Céline Moutou, et al.
Human Mutation|October 28, 2014
An augmented ABCA4 screen targeting noncoding regions reveals a deep intronic founder variant in Belgian Stargardt patientsMiriam Bauwens, Julie De Zaeytijd, Nicole Weisschuh, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

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Pageof 2
Journal of Perinatal Medicine|October 27, 2025
Diagnostic yield and clinical impact of prenatal whole exome sequencing (WES) - four-year single center experienceKatleen Janssens, Marjan De Rademaeker, Joke Muys, et al.
Diagnostics (Basel, Switzerland)|March 11, 2023
Implementation of Exome Sequencing in Prenatal Diagnostics: Chances and ChallengesEwa Janicki, Marjan De Rademaeker, Colombine Meunier, et al.
Clinical Genetics|October 22, 2024
RNU4-2-Related Neurodevelopmental Disorder Is Associated With a Recognisable Facial GestaltJessica Rosenblum, Diane Beysen, Anna C Jansen, et al.
Clinical Case Reports|April 12, 2017
Risk of malignancy in 22q11.2 deletion syndromeToer Stevens, Jutte van der Werff Ten Bosch, Marjan De Rademaeker, et al.
European Journal of Medical Genetics|March 8, 2025
Paracentric inversion disrupting the SHANK2 geneJolien Huyghebaert, Bregje Christiaenssen, Marjan De Rademaeker, et al.
Journal of Assisted Reproduction and Genetics|March 12, 2010
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 tractWillem Verpoest, Sara Seneca, Marjan De Rademaeker, et al.
European Journal of Human Genetics : EJHG|April 16, 2009
Preimplantation genetic diagnosis for myotonic dystrophy type 1: upon request to childMarjan De Rademaeker, Willem Verpoest, Martine De Rycke, et al.
The Journal of Molecular Diagnostics : JMD|August 28, 2012
Reliable and sensitive detection of fragile X (expanded) alleles in clinical prenatal DNA samples with a fast turnaround timeSara Seneca, Willy Lissens, Kristof Endels, et al.
European Journal of Human Genetics : EJHG|November 11, 2011
Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centresMaartje C Van Rij, Marjan De Rademaeker, Céline Moutou, et al.
Human Mutation|October 28, 2014
An augmented ABCA4 screen targeting noncoding regions reveals a deep intronic founder variant in Belgian Stargardt patientsMiriam Bauwens, Julie De Zaeytijd, Nicole Weisschuh, et al.
Pageof 2