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Maryse Bonduelle

Showing results (41-50 of 54) with videos related to

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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.
BMC Cancer|April 6, 2019
Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer familiesRajendra Bahadur Shahi, Sylvia De Brakeleer, Ben Caljon, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|August 8, 2017
Prolonged Right Ventricular Ejection Delay in Brugada Syndrome Depends on the Type of SCN5A Variant　- Electromechanical Coupling Through Tissue Velocity Imaging as a Bridge Between Genotyping and PhenotypingSophie C H Van Malderen, Dorien Daneels, Dirk Kerkhove, et al.
International Journal of Cardiology|May 13, 2015
Prolonged right ventricular ejection delay identifies high risk patients and gender differences in Brugada syndromeSophie C H Van Malderen, Dirk Kerkhove, Dominic A M J Theuns, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|July 17, 2015
Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada SyndromeUschi Peeters, Fabiana Scornik, Helena Riuró, et al.
Human Mutation|March 19, 2021
More than meets the eye: Expanding and reviewing the clinical and mutational spectrum of brittle cornea syndromeTibbe Dhooge, Tim Van Damme, Delfien Syx, et al.
International Journal of Cardiology|September 23, 2011
Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAADMarjolijn Renard, Bert Callewaert, Machteld Baetens, et al.
Nature Communications|February 9, 2024
Children born after assisted reproduction more commonly carry a mitochondrial genotype associating with low birthweightJoke Mertens, Florence Belva, Aafke P A van Montfoort, et al.
Human Reproduction (Oxford, England)|August 8, 2018
Preimplantation genetic testing for aneuploidy by microarray analysis of polar bodies in advanced maternal age: a randomized clinical trialWillem Verpoest, Catherine Staessen, Patrick M Bossuyt, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
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.
BMC Cancer|April 6, 2019
Identification of candidate cancer predisposing variants by performing whole-exome sequencing on index patients from BRCA1 and BRCA2-negative breast cancer familiesRajendra Bahadur Shahi, Sylvia De Brakeleer, Ben Caljon, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|August 8, 2017
Prolonged Right Ventricular Ejection Delay in Brugada Syndrome Depends on the Type of SCN5A Variant　- Electromechanical Coupling Through Tissue Velocity Imaging as a Bridge Between Genotyping and PhenotypingSophie C H Van Malderen, Dorien Daneels, Dirk Kerkhove, et al.
International Journal of Cardiology|May 13, 2015
Prolonged right ventricular ejection delay identifies high risk patients and gender differences in Brugada syndromeSophie C H Van Malderen, Dirk Kerkhove, Dominic A M J Theuns, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|July 17, 2015
Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada SyndromeUschi Peeters, Fabiana Scornik, Helena Riuró, et al.
Human Mutation|March 19, 2021
More than meets the eye: Expanding and reviewing the clinical and mutational spectrum of brittle cornea syndromeTibbe Dhooge, Tim Van Damme, Delfien Syx, et al.
International Journal of Cardiology|September 23, 2011
Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAADMarjolijn Renard, Bert Callewaert, Machteld Baetens, et al.
Nature Communications|February 9, 2024
Children born after assisted reproduction more commonly carry a mitochondrial genotype associating with low birthweightJoke Mertens, Florence Belva, Aafke P A van Montfoort, et al.
Human Reproduction (Oxford, England)|August 8, 2018
Preimplantation genetic testing for aneuploidy by microarray analysis of polar bodies in advanced maternal age: a randomized clinical trialWillem Verpoest, Catherine Staessen, Patrick M Bossuyt, et al.
Pageof 6