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European Journal of Human Genetics : EJHG
|
June 14, 2012
Agenesis of the corpus callosum and gray matter heterotopia in three patients with constitutional mismatch repair deficiency syndrome
Annette F Baas, Michael Gabbett, Milan Rimac, et al.
Atherosclerosis
|
April 3, 2021
Genotype-phenotype correlation in pseudoxanthoma elasticum
Jonas W Bartstra, Sara Risseeuw, Pim A de Jong, et al.
Circulation. Genomic and Precision Medicine
|
October 20, 2022
Prevalence and Disease Expression of Pathogenic and Likely Pathogenic Variants Associated With Inherited Cardiomyopathies in the General Population
Mimount Bourfiss, Marion van Vugt, Abdulrahman I Alasiri, et al.
Circulation. Genomic and Precision Medicine
|
January 22, 2025
Family Screening in Patients With Dilated and Arrhythmogenic Cardiomyopathy: The Road Toward Gene-Specific Recommendations
Sophie L V M Stroeks, Steven Muller, Nina J Beelen, et al.
American Journal of Medical Genetics. Part A
|
January 20, 2017
Six uneventful pregnancy outcomes in an extended vascular Ehlers-Danlos syndrome family
Annette F Baas, Wilko Spiering, Frans L Moll, et al.
The Journal of Cardiovascular Surgery
|
February 7, 2015
Rationale and design of the extracranial Carotid artery Aneurysm Registry (CAR)
Janna C Welleweerd, Michiel L Bots, L Jaap Kappelle, 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.
European Journal of Human Genetics : EJHG
|
April 6, 2017
Genetic variants associated with type 2 diabetes and adiposity and risk of intracranial and abdominal aortic aneurysms
Femke Ng van 't Hof, Julien Vaucher, Michael V Holmes, et al.
American Journal of Medical Genetics. Part A
|
April 8, 2015
Familial Ehlers-Danlos syndrome with lethal arterial events caused by a mutation in COL5A1
Glen R Monroe, Magdalena Harakalova, Saskia N van der Crabben, et al.
Cells
|
November 27, 2021
Distinct Metabolomic Signatures in Preclinical and Obstructive Hypertrophic Cardiomyopathy
Maike Schuldt, Beau van Driel, Sila Algül, et al.
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of 8
Search research articles
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Showing results (31-40 of 71) with videos related to
Sort By:
Page
of 8
European Journal of Human Genetics : EJHG
|
June 14, 2012
Agenesis of the corpus callosum and gray matter heterotopia in three patients with constitutional mismatch repair deficiency syndrome
Annette F Baas, Michael Gabbett, Milan Rimac, et al.
Atherosclerosis
|
April 3, 2021
Genotype-phenotype correlation in pseudoxanthoma elasticum
Jonas W Bartstra, Sara Risseeuw, Pim A de Jong, et al.
Circulation. Genomic and Precision Medicine
|
October 20, 2022
Prevalence and Disease Expression of Pathogenic and Likely Pathogenic Variants Associated With Inherited Cardiomyopathies in the General Population
Mimount Bourfiss, Marion van Vugt, Abdulrahman I Alasiri, et al.
Circulation. Genomic and Precision Medicine
|
January 22, 2025
Family Screening in Patients With Dilated and Arrhythmogenic Cardiomyopathy: The Road Toward Gene-Specific Recommendations
Sophie L V M Stroeks, Steven Muller, Nina J Beelen, et al.
American Journal of Medical Genetics. Part A
|
January 20, 2017
Six uneventful pregnancy outcomes in an extended vascular Ehlers-Danlos syndrome family
Annette F Baas, Wilko Spiering, Frans L Moll, et al.
The Journal of Cardiovascular Surgery
|
February 7, 2015
Rationale and design of the extracranial Carotid artery Aneurysm Registry (CAR)
Janna C Welleweerd, Michiel L Bots, L Jaap Kappelle, 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.
European Journal of Human Genetics : EJHG
|
April 6, 2017
Genetic variants associated with type 2 diabetes and adiposity and risk of intracranial and abdominal aortic aneurysms
Femke Ng van 't Hof, Julien Vaucher, Michael V Holmes, et al.
American Journal of Medical Genetics. Part A
|
April 8, 2015
Familial Ehlers-Danlos syndrome with lethal arterial events caused by a mutation in COL5A1
Glen R Monroe, Magdalena Harakalova, Saskia N van der Crabben, et al.
Cells
|
November 27, 2021
Distinct Metabolomic Signatures in Preclinical and Obstructive Hypertrophic Cardiomyopathy
Maike Schuldt, Beau van Driel, Sila Algül, et al.
Page
of 8