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K te Velde

Showing results (11-20 of 14) with videos related to

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European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies|July 1, 1995
Evaluation and clinical application of the Enterotest for the determination of human biliary porphyrin compositionG J Beukeveld, C M Bijleveld, F Kuipers, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1989
Tissue-specific splicing mutation in acute intermittent porphyriaB Grandchamp, C Picat, V Mignotte, et al.
Human Mutation|January 15, 1999
Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation updateR Rosipal, J Lamoril, H Puy, et al.
The British Journal of Dermatology|September 14, 2011
Extended haplotype studies in South African and Dutch variegate porphyria families carrying the recurrent p.R59W mutation confirm a common ancestryA M van Tuyll van Serooskerken, B I Drögemöller, K Te Velde, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies|July 1, 1995
Evaluation and clinical application of the Enterotest for the determination of human biliary porphyrin compositionG J Beukeveld, C M Bijleveld, F Kuipers, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1989
Tissue-specific splicing mutation in acute intermittent porphyriaB Grandchamp, C Picat, V Mignotte, et al.
Human Mutation|January 15, 1999
Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation updateR Rosipal, J Lamoril, H Puy, et al.
The British Journal of Dermatology|September 14, 2011
Extended haplotype studies in South African and Dutch variegate porphyria families carrying the recurrent p.R59W mutation confirm a common ancestryA M van Tuyll van Serooskerken, B I Drögemöller, K Te Velde, et al.
Pageof 2