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Janine Genschel

Showing results (1-10 of 13) with videos related to

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Human Mutation|November 4, 2004
LDL-receptor mutations in EuropeGeorge V Z Dedoussis, Hartmut Schmidt, Janine Genschel
Cardiology|November 13, 2004
LMNA mutations in cardiac transplant recipientsKlaus Pethig, Janine Genschel, Tina Peters, et al.
World Journal of Gastroenterology|January 8, 2005
NOD2/CARD15 gene polymorphism in patients with inflammatory bowel disease: is Hungary different?Carsten Büning, Tomas Molnar, Ferenc Nagy, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 8, 2005
p.H1069Q mutation in ATP7B and biochemical parameters of copper metabolism and clinical manifestation of Wilson's diseaseGraznya Gromadzka, Harmut H J Schmidt, Janine Genschel, et al.
Parkinsonism & Related Disorders|September 28, 2007
Neurological manifestations and ATP7B mutations in Wilson's diseaseAlexandre Aluizio Costa Machado, Marta Mitiko Deguti, Janine Genschel, et al.
The American Journal of Gastroenterology|September 27, 2005
Hepatic steatosis in Dunnigan-type familial partial lipodystrophyAngelika Lüdtke, Janine Genschel, Georg Brabant, et al.
Digestion|July 19, 2005
Introducing genetic testing for adult-type hypolactasiaCarsten Büning, Janine Genschel, Juliane Jurga, et al.
Human Mutation|March 17, 2004
Wilson disease: novel mutations in the ATP7B gene and clinical correlation in Brazilian patientsMarta M Deguti, Janine Genschel, Eduardo L R Cancado, et al.
Human Mutation|February 20, 2004
Molecular characterization of familial hypercholesterolemia in German and Greek patientsGeorge V Z Dedoussis, Janine Genschel, Bettina Bochow, et al.
Gastroenterology|March 5, 2002
A homozygous HFE gene splice site mutation (IVS5+1 G/A) in a hereditary hemochromatosis patient of Vietnamese originMichael Steiner, Kenneth Ocran, Janine Genschel, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Human Mutation|November 4, 2004
LDL-receptor mutations in EuropeGeorge V Z Dedoussis, Hartmut Schmidt, Janine Genschel
Cardiology|November 13, 2004
LMNA mutations in cardiac transplant recipientsKlaus Pethig, Janine Genschel, Tina Peters, et al.
World Journal of Gastroenterology|January 8, 2005
NOD2/CARD15 gene polymorphism in patients with inflammatory bowel disease: is Hungary different?Carsten Büning, Tomas Molnar, Ferenc Nagy, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 8, 2005
p.H1069Q mutation in ATP7B and biochemical parameters of copper metabolism and clinical manifestation of Wilson's diseaseGraznya Gromadzka, Harmut H J Schmidt, Janine Genschel, et al.
Parkinsonism & Related Disorders|September 28, 2007
Neurological manifestations and ATP7B mutations in Wilson's diseaseAlexandre Aluizio Costa Machado, Marta Mitiko Deguti, Janine Genschel, et al.
The American Journal of Gastroenterology|September 27, 2005
Hepatic steatosis in Dunnigan-type familial partial lipodystrophyAngelika Lüdtke, Janine Genschel, Georg Brabant, et al.
Digestion|July 19, 2005
Introducing genetic testing for adult-type hypolactasiaCarsten Büning, Janine Genschel, Juliane Jurga, et al.
Human Mutation|March 17, 2004
Wilson disease: novel mutations in the ATP7B gene and clinical correlation in Brazilian patientsMarta M Deguti, Janine Genschel, Eduardo L R Cancado, et al.
Human Mutation|February 20, 2004
Molecular characterization of familial hypercholesterolemia in German and Greek patientsGeorge V Z Dedoussis, Janine Genschel, Bettina Bochow, et al.
Gastroenterology|March 5, 2002
A homozygous HFE gene splice site mutation (IVS5+1 G/A) in a hereditary hemochromatosis patient of Vietnamese originMichael Steiner, Kenneth Ocran, Janine Genschel, et al.
Pageof 2