C A van Bennekom - JoVE Visualize

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Clinical Genetics|November 1, 1979

Heterozygote detection in glucose-6-phosphate dehydrogenase deficiency: limitation of hair follicle analysisA J Vermorken, G T Spierenburg, C A van Bennekom, et al.

American Journal of Medical Genetics|February 1, 1991

Multipoint linkage analysis of DXS369 and DXS304 in fragile X familiesB A van Oost, A Smits, J C Dreesen, et al.

Clinical Science (London, England : 1979)|April 1, 1986

Ischaemic exercise test in myoadenylate deaminase deficiency and McArdle's disease: measurement of plasma adenosine, inosine and hypoxanthineS P Sinkeler, E M Joosten, R A Wevers, et al.

Genomics|January 1, 1990

New polymorphic DNA marker close to the fragile site FRAXAB A Oostra, P E Hupkes, L F Perdon, et al.

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

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You have reached the last page of results.This site can display upto 14 results.

Clinical Genetics|November 1, 1979

Heterozygote detection in glucose-6-phosphate dehydrogenase deficiency: limitation of hair follicle analysisA J Vermorken, G T Spierenburg, C A van Bennekom, et al.

American Journal of Medical Genetics|February 1, 1991

Multipoint linkage analysis of DXS369 and DXS304 in fragile X familiesB A van Oost, A Smits, J C Dreesen, et al.

Clinical Science (London, England : 1979)|April 1, 1986

Ischaemic exercise test in myoadenylate deaminase deficiency and McArdle's disease: measurement of plasma adenosine, inosine and hypoxanthineS P Sinkeler, E M Joosten, R A Wevers, et al.

Genomics|January 1, 1990

New polymorphic DNA marker close to the fragile site FRAXAB A Oostra, P E Hupkes, L F Perdon, et al.

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