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Ingrid M B H van de Laar

Showing results (1-10 of 51) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|October 13, 2011
[22q11.2 deletion syndrome diagnosed in an adult male]Robert-Jan Hassing, Judith M A Verhagen, Ingrid M B H van de Laar, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 23, 2013
[Patients with aneurysms and osteoarthritis: Marfan syndrome ruled out, so what is it?]Denise van der Linde, Ingrid M B H van de Laar, Adriaan Moelker, et al.
Child Neurology Open|November 11, 2021
Expanding Phenotype of <i>ATP1A3</i> - Related Disorders: A Case SeriesJelena De Vrieze, Ingrid M B H van de Laar, Johanneke F de Rijk-van Andel, et al.
Journal of Vascular Surgery|September 15, 2012
Aneurysm-osteoarthritis syndrome with visceral and iliac artery aneurysmsDenise van der Linde, Hence J M Verhagen, Adriaan Moelker, et al.
Cardiovascular Research|June 4, 2010
Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndromeCornelis J J Boogerd, Dennis Dooijes, Aho Ilgun, et al.
Journal of Human Genetics|November 27, 2015
Broadening the phenotypic spectrum of pathogenic LARP7 variants: two cases with intellectual disability, variable growth retardation and distinct facial featuresIris H I M Hollink, Majid Alfadhel, Anwar S Al-Wakeel, et al.
Journal of Human Genetics|March 27, 2018
Correction: Broadening the phenotypic spectrum of pathogenic LARP7 variants: two cases with intellectual disability, variable growth retardation and distinct facial featuresIris H I M Hollink, Majid Alfadhel, Anwar S Al-Wakeel, et al.
American Journal of Medical Genetics. Part A|May 28, 2019
Psychological well-being in patients with aneurysms-osteoarthritis syndromeLidia R Bons, Allard T van den Hoven, Ayda E Damirchi, et al.
American Journal of Medical Genetics. Part A|January 24, 2009
Autosomal dominant inheritance of cardiac valves anomalies in two families: extended spectrum of left-ventricular outflow tract obstructionMarja W Wessels, Ingrid M B H van de Laar, Jolien Roos-Hesselink, et al.
European Journal of Medical Genetics|July 2, 2022
Surveillance and monitoring in vascular Ehlers-Danlos syndrome in European Reference Network For Rare Vascular Diseases (VASCERN)Ingrid M B H van de Laar, Annette F Baas, Julie De Backer, et al.
Pageof 6

Showing results (1-10 of 51) with videos related to

Sort By:
Pageof 6
Nederlands Tijdschrift Voor Geneeskunde|October 13, 2011
[22q11.2 deletion syndrome diagnosed in an adult male]Robert-Jan Hassing, Judith M A Verhagen, Ingrid M B H van de Laar, et al.
Nederlands Tijdschrift Voor Geneeskunde|May 23, 2013
[Patients with aneurysms and osteoarthritis: Marfan syndrome ruled out, so what is it?]Denise van der Linde, Ingrid M B H van de Laar, Adriaan Moelker, et al.
Child Neurology Open|November 11, 2021
Expanding Phenotype of <i>ATP1A3</i> - Related Disorders: A Case SeriesJelena De Vrieze, Ingrid M B H van de Laar, Johanneke F de Rijk-van Andel, et al.
Journal of Vascular Surgery|September 15, 2012
Aneurysm-osteoarthritis syndrome with visceral and iliac artery aneurysmsDenise van der Linde, Hence J M Verhagen, Adriaan Moelker, et al.
Cardiovascular Research|June 4, 2010
Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndromeCornelis J J Boogerd, Dennis Dooijes, Aho Ilgun, et al.
Journal of Human Genetics|November 27, 2015
Broadening the phenotypic spectrum of pathogenic LARP7 variants: two cases with intellectual disability, variable growth retardation and distinct facial featuresIris H I M Hollink, Majid Alfadhel, Anwar S Al-Wakeel, et al.
Journal of Human Genetics|March 27, 2018
Correction: Broadening the phenotypic spectrum of pathogenic LARP7 variants: two cases with intellectual disability, variable growth retardation and distinct facial featuresIris H I M Hollink, Majid Alfadhel, Anwar S Al-Wakeel, et al.
American Journal of Medical Genetics. Part A|May 28, 2019
Psychological well-being in patients with aneurysms-osteoarthritis syndromeLidia R Bons, Allard T van den Hoven, Ayda E Damirchi, et al.
American Journal of Medical Genetics. Part A|January 24, 2009
Autosomal dominant inheritance of cardiac valves anomalies in two families: extended spectrum of left-ventricular outflow tract obstructionMarja W Wessels, Ingrid M B H van de Laar, Jolien Roos-Hesselink, et al.
European Journal of Medical Genetics|July 2, 2022
Surveillance and monitoring in vascular Ehlers-Danlos syndrome in European Reference Network For Rare Vascular Diseases (VASCERN)Ingrid M B H van de Laar, Annette F Baas, Julie De Backer, et al.
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