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M Mannens

Showing results (31-40 of 172) with videos related to

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Molecular Cytogenetics|November 29, 2023
Prenatal identification of an inverted duplicated 13q marker chromosome with a neocentromereLiselot van der Laan, Daniel R Hoekman, Esther J Wortelboer, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|May 6, 2017
Transthyretin amyloidosis: a phenocopy of hypertrophic cardiomyopathyAlexa M C Vermeer, Anneloes Janssen, Peter C Boorsma, et al.
Journal of Medical Genetics|December 1, 1995
Further delineation of the partial proximal trisomy 10q syndromeC M Aalfs, J M Hoovers, M A Nieste-Otter, et al.
European Journal of Human Genetics : EJHG|July 26, 2000
Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studiesR van den Bogaard, C A Fijen, M G Schipper, et al.
Human Genetics|August 15, 2000
Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3A V Postma, C R Bezzina, J F de Vries, et al.
Cytogenetics and Cell Genetics|June 1, 2000
Delineation and physical separation of novel translocation breakpoints on chromosome 1p in two genetically closely associated childhood tumorsM J Steenman, N Zijlstra, D L Kruitbosch, et al.
American Journal of Human Genetics|April 14, 2000
Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndromeM Alders, A Ryan, M Hodges, et al.
Human Molecular Genetics|March 1, 1995
Aniridia-associated cytogenetic rearrangements suggest that a position effect may cause the mutant phenotypeJ Fantes, B Redeker, M Breen, et al.
Nutrients|October 31, 2018
Higher Polygenetic Predisposition for Asthma in Cow's Milk Allergic ChildrenPhilip R Jansen, Nicole C M Petrus, Andrea Venema, et al.
Heart Rhythm|August 1, 2006
Arrhythmogenic right ventricular cardiomyopathy due to a novel plakophilin 2 mutation: wide spectrum of disease in mutation carriers within a familyPrince J Kannankeril, Zahurul A Bhuiyan, Dawood Darbar, et al.
Pageof 18

Showing results (31-40 of 172) with videos related to

Sort By:
Pageof 18
Molecular Cytogenetics|November 29, 2023
Prenatal identification of an inverted duplicated 13q marker chromosome with a neocentromereLiselot van der Laan, Daniel R Hoekman, Esther J Wortelboer, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|May 6, 2017
Transthyretin amyloidosis: a phenocopy of hypertrophic cardiomyopathyAlexa M C Vermeer, Anneloes Janssen, Peter C Boorsma, et al.
Journal of Medical Genetics|December 1, 1995
Further delineation of the partial proximal trisomy 10q syndromeC M Aalfs, J M Hoovers, M A Nieste-Otter, et al.
European Journal of Human Genetics : EJHG|July 26, 2000
Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studiesR van den Bogaard, C A Fijen, M G Schipper, et al.
Human Genetics|August 15, 2000
Genomic organisation and chromosomal localisation of two members of the KCND ion channel family, KCND2 and KCND3A V Postma, C R Bezzina, J F de Vries, et al.
Cytogenetics and Cell Genetics|June 1, 2000
Delineation and physical separation of novel translocation breakpoints on chromosome 1p in two genetically closely associated childhood tumorsM J Steenman, N Zijlstra, D L Kruitbosch, et al.
American Journal of Human Genetics|April 14, 2000
Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndromeM Alders, A Ryan, M Hodges, et al.
Human Molecular Genetics|March 1, 1995
Aniridia-associated cytogenetic rearrangements suggest that a position effect may cause the mutant phenotypeJ Fantes, B Redeker, M Breen, et al.
Nutrients|October 31, 2018
Higher Polygenetic Predisposition for Asthma in Cow's Milk Allergic ChildrenPhilip R Jansen, Nicole C M Petrus, Andrea Venema, et al.
Heart Rhythm|August 1, 2006
Arrhythmogenic right ventricular cardiomyopathy due to a novel plakophilin 2 mutation: wide spectrum of disease in mutation carriers within a familyPrince J Kannankeril, Zahurul A Bhuiyan, Dawood Darbar, et al.
Pageof 18