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Christiane Zweier

Showing results (1-10 of 164) with videos related to

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Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 10, 2024
Modelling phenotypes, variants and pathomechanisms of syndromic diseases in different systemsAnne Gregor, Christiane Zweier
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|July 21, 2025
Precision medicineChristiane Zweier, Miriam Elbracht, Ilona Krey-Grauert
Circulation. Genomic and Precision Medicine|June 16, 2023
Novel Insights Into the Prevalence of <i>TNNI3K</i>-Mediated Dilated Cardiomyopathy and Putative Disease MechanismsMarina Rieder, Christiane Zweier, Katja E Odening
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|July 21, 2025
Editorial - Patient perspectives on new therapies for genetic diseasesMiriam Elbracht, Christiane Zweier, Ilona Krey-Grauert
American Journal of Medical Genetics. Part A|March 15, 2006
Atypical ZFHX1B mutation associated with a mild Mowat-Wilson syndrome phenotypeChristiane Zweier, Denise Horn, Cornelia Kraus, et al.
American Journal of Medical Genetics. Part A|December 18, 2003
Facial phenotype allows diagnosis of Mowat-Wilson syndrome in the absence of Hirschsprung diseaseDenise Horn, Bernhard Weschke, Christiane Zweier, et al.
European Journal of Medical Genetics|March 18, 2008
A 15Mb duplication of 6q24.1-q25.3 associated with typical but milder features of the duplication 6q syndromeChristiane Zweier, Udo Trautmann, Arif Ekici, et al.
American Journal of Medical Genetics. Part A|June 9, 2012
De novo triplication of the MAPT gene from the recurrent 17q21.31 microdeletion region in a patient with moderate intellectual disability and various minor anomaliesAnne Gregor, Mandy Krumbiegel, Cornelia Kraus, et al.
European Journal of Medical Genetics|September 24, 2005
9 Mb deletion including chromosome band 3q24 associated with unsuspicious facial gestalt, persistent ductus omphaloentericus, mild mental retardation and ticChristiane Zweier, Sabine Guth, Uta Schulte-Mattler, et al.
Disease Models & Mechanisms|May 16, 2019
Intellectual disability and autism spectrum disorders 'on the fly': insights from <i>Drosophila</i>Mireia Coll-Tané, Alina Krebbers, Anna Castells-Nobau, et al.
Pageof 17

Showing results (1-10 of 164) with videos related to

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Pageof 17
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 10, 2024
Modelling phenotypes, variants and pathomechanisms of syndromic diseases in different systemsAnne Gregor, Christiane Zweier
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|July 21, 2025
Precision medicineChristiane Zweier, Miriam Elbracht, Ilona Krey-Grauert
Circulation. Genomic and Precision Medicine|June 16, 2023
Novel Insights Into the Prevalence of <i>TNNI3K</i>-Mediated Dilated Cardiomyopathy and Putative Disease MechanismsMarina Rieder, Christiane Zweier, Katja E Odening
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|July 21, 2025
Editorial - Patient perspectives on new therapies for genetic diseasesMiriam Elbracht, Christiane Zweier, Ilona Krey-Grauert
American Journal of Medical Genetics. Part A|March 15, 2006
Atypical ZFHX1B mutation associated with a mild Mowat-Wilson syndrome phenotypeChristiane Zweier, Denise Horn, Cornelia Kraus, et al.
American Journal of Medical Genetics. Part A|December 18, 2003
Facial phenotype allows diagnosis of Mowat-Wilson syndrome in the absence of Hirschsprung diseaseDenise Horn, Bernhard Weschke, Christiane Zweier, et al.
European Journal of Medical Genetics|March 18, 2008
A 15Mb duplication of 6q24.1-q25.3 associated with typical but milder features of the duplication 6q syndromeChristiane Zweier, Udo Trautmann, Arif Ekici, et al.
American Journal of Medical Genetics. Part A|June 9, 2012
De novo triplication of the MAPT gene from the recurrent 17q21.31 microdeletion region in a patient with moderate intellectual disability and various minor anomaliesAnne Gregor, Mandy Krumbiegel, Cornelia Kraus, et al.
European Journal of Medical Genetics|September 24, 2005
9 Mb deletion including chromosome band 3q24 associated with unsuspicious facial gestalt, persistent ductus omphaloentericus, mild mental retardation and ticChristiane Zweier, Sabine Guth, Uta Schulte-Mattler, et al.
Disease Models & Mechanisms|May 16, 2019
Intellectual disability and autism spectrum disorders 'on the fly': insights from <i>Drosophila</i>Mireia Coll-Tané, Alina Krebbers, Anna Castells-Nobau, et al.
Pageof 17