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M Mannens

Showing results (61-70 of 172) with videos related to

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European Journal of Medical Genetics|September 9, 2009
Phenotypic discordance upon paternal or maternal transmission of duplications of the 11p15 imprinted regionsJ Bliek, S Snijder, S M Maas, et al.
Human Genetics|February 1, 1987
Regional localization of DNA probes on the short arm of chromosome 11 using aniridia-Wilms' tumor-associated deletionsM Mannens, R M Slater, C Heyting, et al.
Circulation|May 26, 2004
Mutation in the KCNQ1 gene leading to the short QT-interval syndromeChloé Bellocq, Antoni C G van Ginneken, Connie R Bezzina, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch familyM Mannens, E M Bleeker-Wagemakers, J Bliek, et al.
The Journal of Biological Chemistry|April 18, 1998
A dominant negative isoform of the long QT syndrome 1 gene productS Demolombe, I Baró, Y Péréon, et al.
Clinical Genetics|March 29, 2000
Molecular genetic testing for familial hypercholesterolemia: spectrum of LDL receptor gene mutations in The NetherlandsM P Lombardi, E J Redeker, J C Defesche, et al.
Translational Psychiatry|July 26, 2024
Distinct saliva DNA methylation profiles in relation to treatment outcome in youth with posttraumatic stress disorderJudith B M Ensink, Peter Henneman, Andrea Venema, et al.
Obesity Reviews : an Official Journal of the International Association for the Study of Obesity|July 29, 2024
The utility of obesity polygenic risk scores from research to clinical practice: A reviewPhilip R Jansen, Niels Vos, Jorrit van Uhm, et al.
Cardiovascular Research|February 26, 2000
Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndromeM B Rook, C Bezzina Alshinawi, W A Groenewegen, et al.
Genomics|October 1, 1991
The distal region of 11p13 and associated genetic diseasesM Mannens, J M Hoovers, E M Bleeker-Wagemakers, et al.
Pageof 18

Showing results (61-70 of 172) with videos related to

Sort By:
Pageof 18
European Journal of Medical Genetics|September 9, 2009
Phenotypic discordance upon paternal or maternal transmission of duplications of the 11p15 imprinted regionsJ Bliek, S Snijder, S M Maas, et al.
Human Genetics|February 1, 1987
Regional localization of DNA probes on the short arm of chromosome 11 using aniridia-Wilms' tumor-associated deletionsM Mannens, R M Slater, C Heyting, et al.
Circulation|May 26, 2004
Mutation in the KCNQ1 gene leading to the short QT-interval syndromeChloé Bellocq, Antoni C G van Ginneken, Connie R Bezzina, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch familyM Mannens, E M Bleeker-Wagemakers, J Bliek, et al.
The Journal of Biological Chemistry|April 18, 1998
A dominant negative isoform of the long QT syndrome 1 gene productS Demolombe, I Baró, Y Péréon, et al.
Clinical Genetics|March 29, 2000
Molecular genetic testing for familial hypercholesterolemia: spectrum of LDL receptor gene mutations in The NetherlandsM P Lombardi, E J Redeker, J C Defesche, et al.
Translational Psychiatry|July 26, 2024
Distinct saliva DNA methylation profiles in relation to treatment outcome in youth with posttraumatic stress disorderJudith B M Ensink, Peter Henneman, Andrea Venema, et al.
Obesity Reviews : an Official Journal of the International Association for the Study of Obesity|July 29, 2024
The utility of obesity polygenic risk scores from research to clinical practice: A reviewPhilip R Jansen, Niels Vos, Jorrit van Uhm, et al.
Cardiovascular Research|February 26, 2000
Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndromeM B Rook, C Bezzina Alshinawi, W A Groenewegen, et al.
Genomics|October 1, 1991
The distal region of 11p13 and associated genetic diseasesM Mannens, J M Hoovers, E M Bleeker-Wagemakers, et al.
Pageof 18