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Gerard J te Meerman

Showing results (51-60 of 57) with videos related to

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Journal of the American College of Cardiology|June 30, 2007
Severe myocardial fibrosis caused by a deletion of the 5' end of the lamin A/C geneJ Peter van Tintelen, Rene A Tio, Wilhelmina S Kerstjens-Frederikse, et al.
American Journal of Human Genetics|August 29, 2017
Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted HaplotypingCarlo Vermeulen, Geert Geeven, Elzo de Wit, et al.
European Journal of Human Genetics : EJHG|April 26, 2002
The ABCA4 2588G>C Stargardt mutation: single origin and increasing frequency from South-West to North-East EuropeAlessandra Maugeri, Kris Flothmann, Nadine Hemmrich, et al.
Plos Genetics|August 11, 2011
Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLARudolf S N Fehrmann, Ritsert C Jansen, Jan H Veldink, et al.
Circulation. Cardiovascular Genetics|August 10, 2017
<i>Lamin A/C</i>-Related Cardiac Disease: Late Onset With a Variable and Mild Phenotype in a Large Cohort of Patients With the Lamin A/C p.(Arg331Gln) Founder MutationEdgar T Hoorntje, Ilse A Bollen, Daniela Q Barge-Schaapveld, et al.
The New England Journal of Medicine|October 4, 2013
PLS3 mutations in X-linked osteoporosis with fracturesFleur S van Dijk, M Carola Zillikens, Dimitra Micha, et al.
Circulation. Genomic and Precision Medicine|December 29, 2022
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (<i>DSP</i>) Truncating VariantEdgar T Hoorntje, Charlotte Burns, Luisa Marsili, et al.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
Journal of the American College of Cardiology|June 30, 2007
Severe myocardial fibrosis caused by a deletion of the 5' end of the lamin A/C geneJ Peter van Tintelen, Rene A Tio, Wilhelmina S Kerstjens-Frederikse, et al.
American Journal of Human Genetics|August 29, 2017
Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted HaplotypingCarlo Vermeulen, Geert Geeven, Elzo de Wit, et al.
European Journal of Human Genetics : EJHG|April 26, 2002
The ABCA4 2588G>C Stargardt mutation: single origin and increasing frequency from South-West to North-East EuropeAlessandra Maugeri, Kris Flothmann, Nadine Hemmrich, et al.
Plos Genetics|August 11, 2011
Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLARudolf S N Fehrmann, Ritsert C Jansen, Jan H Veldink, et al.
Circulation. Cardiovascular Genetics|August 10, 2017
<i>Lamin A/C</i>-Related Cardiac Disease: Late Onset With a Variable and Mild Phenotype in a Large Cohort of Patients With the Lamin A/C p.(Arg331Gln) Founder MutationEdgar T Hoorntje, Ilse A Bollen, Daniela Q Barge-Schaapveld, et al.
The New England Journal of Medicine|October 4, 2013
PLS3 mutations in X-linked osteoporosis with fracturesFleur S van Dijk, M Carola Zillikens, Dimitra Micha, et al.
Circulation. Genomic and Precision Medicine|December 29, 2022
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (<i>DSP</i>) Truncating VariantEdgar T Hoorntje, Charlotte Burns, Luisa Marsili, et al.
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