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M Mannens

Showing results (71-80 of 172) with videos related to

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Journal of Cardiovascular Electrophysiology|August 2, 2007
A novel early onset lethal form of catecholaminergic polymorphic ventricular tachycardia maps to chromosome 7p14-p22Zahurul A Bhuiyan, Mohamed A Hamdan, Eman T A Shamsi, et al.
Heart Rhythm|June 9, 2007
Exclusion of multiple candidate genes and large genomic rearrangements in SCN5A in a Dutch Brugada syndrome cohortTamara T Koopmann, Leander Beekman, Marielle Alders, et al.
Circulation Research|October 19, 2002
Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardiaAlex V Postma, Isabelle Denjoy, Theo M Hoorntje, et al.
European Journal of Medical Genetics|April 8, 2014
Methylation analysis in tongue tissue of BWS patients identifies the (EPI)genetic cause in 3 patients with normal methylation levels in bloodMariëlle Alders, Saskia M Maas, Daniël J M Kadouch, et al.
Cardiovascular Research|March 26, 2003
A novel LQT3 mutation implicates the human cardiac sodium channel domain IVS6 in inactivation kineticsW Antoinette Groenewegen, Connie R Bezzina, J Peter van Tintelen, et al.
American Journal of Medical Genetics. Part A|July 16, 2016
Phenotype, cancer risk, and surveillance in Beckwith-Wiedemann syndrome depending on molecular genetic subgroupsSaskia M Maas, Fleur Vansenne, Daniel J M Kadouch, et al.
The Journal of General Virology|February 1, 1988
Morphological transformation by early region human polyomavirus BK DNA of human fibroblasts with deletions in the short arm of one chromosome 11A de Ronde, M Mannens, R M Slater, et al.
Human Molecular Genetics|June 1, 1997
The human Achaete-Scute homologue 2 (ASCL2,HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillus trophoblastsM Alders, M Hodges, A K Hadjantonakis, et al.
Pediatric Cardiology|February 3, 2009
Clinical and genetic analysis of long QT syndrome in children from six families in Saudi Arabia: are they different?Zahurul A Bhuiyan, Safar Al-Shahrani, Ayman S Al-Khadra, et al.
Journal of Community Genetics|March 22, 2021
Clinical and community genetics services in the Dutch CaribbeanEline A Verberne, Ginette M Ecury-Goossen, Meindert E Manshande, et al.
Pageof 18

Showing results (71-80 of 172) with videos related to

Sort By:
Pageof 18
Journal of Cardiovascular Electrophysiology|August 2, 2007
A novel early onset lethal form of catecholaminergic polymorphic ventricular tachycardia maps to chromosome 7p14-p22Zahurul A Bhuiyan, Mohamed A Hamdan, Eman T A Shamsi, et al.
Heart Rhythm|June 9, 2007
Exclusion of multiple candidate genes and large genomic rearrangements in SCN5A in a Dutch Brugada syndrome cohortTamara T Koopmann, Leander Beekman, Marielle Alders, et al.
Circulation Research|October 19, 2002
Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardiaAlex V Postma, Isabelle Denjoy, Theo M Hoorntje, et al.
European Journal of Medical Genetics|April 8, 2014
Methylation analysis in tongue tissue of BWS patients identifies the (EPI)genetic cause in 3 patients with normal methylation levels in bloodMariëlle Alders, Saskia M Maas, Daniël J M Kadouch, et al.
Cardiovascular Research|March 26, 2003
A novel LQT3 mutation implicates the human cardiac sodium channel domain IVS6 in inactivation kineticsW Antoinette Groenewegen, Connie R Bezzina, J Peter van Tintelen, et al.
American Journal of Medical Genetics. Part A|July 16, 2016
Phenotype, cancer risk, and surveillance in Beckwith-Wiedemann syndrome depending on molecular genetic subgroupsSaskia M Maas, Fleur Vansenne, Daniel J M Kadouch, et al.
The Journal of General Virology|February 1, 1988
Morphological transformation by early region human polyomavirus BK DNA of human fibroblasts with deletions in the short arm of one chromosome 11A de Ronde, M Mannens, R M Slater, et al.
Human Molecular Genetics|June 1, 1997
The human Achaete-Scute homologue 2 (ASCL2,HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillus trophoblastsM Alders, M Hodges, A K Hadjantonakis, et al.
Pediatric Cardiology|February 3, 2009
Clinical and genetic analysis of long QT syndrome in children from six families in Saudi Arabia: are they different?Zahurul A Bhuiyan, Safar Al-Shahrani, Ayman S Al-Khadra, et al.
Journal of Community Genetics|March 22, 2021
Clinical and community genetics services in the Dutch CaribbeanEline A Verberne, Ginette M Ecury-Goossen, Meindert E Manshande, et al.
Pageof 18