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Ingrid van de Laar

Showing results (1-10 of 22) with videos related to

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American Journal of Medical Genetics. Part A|October 17, 2007
Limb anomalies in patients with CHARGE syndrome: an expansion of the phenotypeIngrid Van de Laar, Dennis Dooijes, Lies Hoefsloot, et al.
Lancet (London, England)|December 20, 2011
Saccular aneurysm within a persistent ductus arteriosusDenise van der Linde, Maarten Witsenburg, Ingrid van de Laar, et al.
European Heart Journal|October 20, 2007
Cardiac beta-myosin heavy chain defects in two families with non-compaction cardiomyopathy: linking non-compaction to hypertrophic, restrictive, and dilated cardiomyopathiesYvonne M Hoedemaekers, Kadir Caliskan, Danielle Majoor-Krakauer, et al.
Experimental Brain Research|June 9, 2005
Cerebral oxygen saturation and electrical brain activity before, during, and up to 36 hours after arterial switch procedure in neonates without pre-existing brain damage: its relationship to neurodevelopmental outcomeMona C Toet, Annebeth Flinterman, Ingrid van de Laar, et al.
European Journal of Medical Genetics|December 13, 2006
A familial inverted duplication 2q33-q34 identified and delineated by multiple cytogenetic techniquesBert H Eussen, Ingrid van de Laar, Hannie Douben, et al.
European Journal of Preventive Cardiology|June 12, 2019
Genetic counselling and testing in adults with congenital heart disease: A consensus document of the ESC Working Group of Grown-Up Congenital Heart Disease, the ESC Working Group on Aorta and Peripheral Vascular Disease and the European Society of Human GeneticsJulie De Backer, Antoine Bondue, Werner Budts, et al.
Human Mutation|February 24, 2015
Genetic heterogeneity and clinical variability in musculocontractural Ehlers-Danlos syndrome caused by impaired dermatan sulfate biosynthesisDelfien Syx, Tim Van Damme, Sofie Symoens, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
Familial gigantism caused by an NSD1 mutationMieke M van Haelst, Jeannette J M Hoogeboom, Genevieve Baujat, et al.
Neurology|August 10, 2012
PRRT2 phenotypes and penetrance of paroxysmal kinesigenic dyskinesia and infantile convulsionsRianne van Vliet, Guido Breedveld, Johanneke de Rijk-van Andel, et al.
Neurology|February 3, 2022
De Novo <i>ATP1A1</i> Variants in an Early-Onset Complex Neurodevelopmental SyndromeMaike F Dohrn, Adriana P Rebelo, Siddharth Srivastava, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics. Part A|October 17, 2007
Limb anomalies in patients with CHARGE syndrome: an expansion of the phenotypeIngrid Van de Laar, Dennis Dooijes, Lies Hoefsloot, et al.
Lancet (London, England)|December 20, 2011
Saccular aneurysm within a persistent ductus arteriosusDenise van der Linde, Maarten Witsenburg, Ingrid van de Laar, et al.
European Heart Journal|October 20, 2007
Cardiac beta-myosin heavy chain defects in two families with non-compaction cardiomyopathy: linking non-compaction to hypertrophic, restrictive, and dilated cardiomyopathiesYvonne M Hoedemaekers, Kadir Caliskan, Danielle Majoor-Krakauer, et al.
Experimental Brain Research|June 9, 2005
Cerebral oxygen saturation and electrical brain activity before, during, and up to 36 hours after arterial switch procedure in neonates without pre-existing brain damage: its relationship to neurodevelopmental outcomeMona C Toet, Annebeth Flinterman, Ingrid van de Laar, et al.
European Journal of Medical Genetics|December 13, 2006
A familial inverted duplication 2q33-q34 identified and delineated by multiple cytogenetic techniquesBert H Eussen, Ingrid van de Laar, Hannie Douben, et al.
European Journal of Preventive Cardiology|June 12, 2019
Genetic counselling and testing in adults with congenital heart disease: A consensus document of the ESC Working Group of Grown-Up Congenital Heart Disease, the ESC Working Group on Aorta and Peripheral Vascular Disease and the European Society of Human GeneticsJulie De Backer, Antoine Bondue, Werner Budts, et al.
Human Mutation|February 24, 2015
Genetic heterogeneity and clinical variability in musculocontractural Ehlers-Danlos syndrome caused by impaired dermatan sulfate biosynthesisDelfien Syx, Tim Van Damme, Sofie Symoens, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
Familial gigantism caused by an NSD1 mutationMieke M van Haelst, Jeannette J M Hoogeboom, Genevieve Baujat, et al.
Neurology|August 10, 2012
PRRT2 phenotypes and penetrance of paroxysmal kinesigenic dyskinesia and infantile convulsionsRianne van Vliet, Guido Breedveld, Johanneke de Rijk-van Andel, et al.
Neurology|February 3, 2022
De Novo <i>ATP1A1</i> Variants in an Early-Onset Complex Neurodevelopmental SyndromeMaike F Dohrn, Adriana P Rebelo, Siddharth Srivastava, et al.
Pageof 3