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Molecular Syndromology
|
October 30, 2013
Otocephaly-Dysgnathia Complex: Description of Four Cases and Confirmation of the Role of OTX2
O Patat, C M A van Ravenswaaij-Arts, J Tantau, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
December 24, 2004
[Arrhythmogenic right-ventricular cardiomyopathy: different manifestations as precursors of sudden death which might be prevented]
P van der Harst, A C P Wiesfeld, I C van Gelder, et al.
American Journal of Medical Genetics. Part A
|
February 4, 2012
Superior mesenteric artery aneurysm in a 9-year-old boy with classical Ehlers-Danlos syndrome
K de Leeuw, J F Goorhuis, I F J Tielliu, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
February 20, 2015
An extended family suddenly confronted with a life-threatening hereditary arrhythmia
K S W H Hendriks, I M van Langen, J P van Tintelen, et al.
Clinical Genetics
|
August 15, 2012
Detection of genomic deletions of PKP2 in arrhythmogenic right ventricular cardiomyopathy
J D Roberts, J C Herkert, J Rutberg, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
December 15, 2018
Prevalence and cardiac phenotype of patients with a phospholamban mutation
I E Hof, J F van der Heijden, E G Kranias, et al.
Community Genetics
|
June 1, 2005
High distress in parents whose children undergo predictive testing for long QT syndrome
Karin S W H Hendriks, F J M Grosfeld, A A M Wilde, et al.
American Journal of Medical Genetics. Part A
|
September 9, 2005
Can parents adjust to the idea that their child is at risk for a sudden death?: Psychological impact of risk for long QT syndrome
Karin S W H Hendriks, F J M Grosfeld, J P van Tintelen, et al.
Journal of the American College of Cardiology
|
February 11, 1999
Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1)
A A Wilde, R J Jongbloed, P A Doevendans, et al.
Human Mutation
|
April 29, 1999
Novel KCNQ1 and HERG missense mutations in Dutch long-QT families
R J Jongbloed, A A Wilde, J L Geelen, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 44) with videos related to
Sort By:
Page
of 5
Molecular Syndromology
|
October 30, 2013
Otocephaly-Dysgnathia Complex: Description of Four Cases and Confirmation of the Role of OTX2
O Patat, C M A van Ravenswaaij-Arts, J Tantau, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
December 24, 2004
[Arrhythmogenic right-ventricular cardiomyopathy: different manifestations as precursors of sudden death which might be prevented]
P van der Harst, A C P Wiesfeld, I C van Gelder, et al.
American Journal of Medical Genetics. Part A
|
February 4, 2012
Superior mesenteric artery aneurysm in a 9-year-old boy with classical Ehlers-Danlos syndrome
K de Leeuw, J F Goorhuis, I F J Tielliu, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
February 20, 2015
An extended family suddenly confronted with a life-threatening hereditary arrhythmia
K S W H Hendriks, I M van Langen, J P van Tintelen, et al.
Clinical Genetics
|
August 15, 2012
Detection of genomic deletions of PKP2 in arrhythmogenic right ventricular cardiomyopathy
J D Roberts, J C Herkert, J Rutberg, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
December 15, 2018
Prevalence and cardiac phenotype of patients with a phospholamban mutation
I E Hof, J F van der Heijden, E G Kranias, et al.
Community Genetics
|
June 1, 2005
High distress in parents whose children undergo predictive testing for long QT syndrome
Karin S W H Hendriks, F J M Grosfeld, A A M Wilde, et al.
American Journal of Medical Genetics. Part A
|
September 9, 2005
Can parents adjust to the idea that their child is at risk for a sudden death?: Psychological impact of risk for long QT syndrome
Karin S W H Hendriks, F J M Grosfeld, J P van Tintelen, et al.
Journal of the American College of Cardiology
|
February 11, 1999
Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1)
A A Wilde, R J Jongbloed, P A Doevendans, et al.
Human Mutation
|
April 29, 1999
Novel KCNQ1 and HERG missense mutations in Dutch long-QT families
R J Jongbloed, A A Wilde, J L Geelen, et al.
Page
of 5