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W J Craigen

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Annals of Neurology|January 23, 1999

D-2-Hydroxyglutaric aciduria: biochemical marker or clinical disease entity?M S van der Knaap, C Jakobs, G F Hoffmann, et al.

Human Mutation|January 22, 2008

Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinaseD P Dimmock, Q Zhang, C Dionisi-Vici, et al.

Human Mutation|April 29, 1998

Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null allelesC J Gallione, D J Klaus, E Y Yeh, et al.

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Search research articles

Showing results (51-60 of 53) with videos related to

Sort By:

Pageof 6

You have reached the last page of results.This site can display upto 53 results.

Annals of Neurology|January 23, 1999

D-2-Hydroxyglutaric aciduria: biochemical marker or clinical disease entity?M S van der Knaap, C Jakobs, G F Hoffmann, et al.

Human Mutation|January 22, 2008

Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinaseD P Dimmock, Q Zhang, C Dionisi-Vici, et al.

Human Mutation|April 29, 1998

Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null allelesC J Gallione, D J Klaus, E Y Yeh, et al.

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