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Annals of Human Genetics|April 23, 2005
Wilson disease: high prevalence in a mountainous area of CreteG V Z Dedoussis, J Genschel, T-E Sialvera, et al.
Clinical Genetics|November 15, 2005
Frameshift and nonsense mutations in the gene for ATPase7B are associated with severe impairment of copper metabolism and with an early clinical manifestation of Wilson's diseaseG Gromadzka, H H-J Schmidt, J Genschel, et al.
Alimentary Pharmacology & Therapeutics|May 15, 2004
Mutations in the NOD2/CARD15 gene in Crohn's disease are associated with ileocecal resection and are a risk factor for reoperationC Büning, J Genschel, S Bühner, et al.
Pageof 1

Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
Annals of Human Genetics|April 23, 2005
Wilson disease: high prevalence in a mountainous area of CreteG V Z Dedoussis, J Genschel, T-E Sialvera, et al.
Clinical Genetics|November 15, 2005
Frameshift and nonsense mutations in the gene for ATPase7B are associated with severe impairment of copper metabolism and with an early clinical manifestation of Wilson's diseaseG Gromadzka, H H-J Schmidt, J Genschel, et al.
Alimentary Pharmacology & Therapeutics|May 15, 2004
Mutations in the NOD2/CARD15 gene in Crohn's disease are associated with ileocecal resection and are a risk factor for reoperationC Büning, J Genschel, S Bühner, et al.
Pageof 1