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M J Kotze

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Blood Cells, Molecules & Diseases|November 27, 1999
Significance of linkage disequilibrium between mutation C282Y and a MseI polymorphism in population screening and DNA diagnosis of hemochromatosisJ N de Villiers, M J Kotze
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|February 16, 2002
Clinical versus molecular diagnosis of heterozygous familial hypercholesterolaemia in the diverse South African populationJ Vergotine, R Thiart, M J Kotze
Molecular and Cellular Probes|February 1, 1995
Screening South African familial adenomatous polyposis families for the five-nucleotide deletion at codon 1309 of the APC geneJ J Grobbelaar, C J Oosthuizen, M J Kotze
Human Genetics|August 1, 1989
Multiple mutations underlying familial hypercholesterolemia in the South African populationH E Henderson, M J Kotze, G M Berger
SADJ : Journal of the South African Dental Association = Tydskrif Van Die Suid-Afrikaanse Tandheelkundige Vereniging|November 29, 2012
A radiological method to evaluate alveolar bone regeneration in the Chacma baboon (Papio ursinus)M J Kotze, K W Bütow, H F Kotze
Human Genetics|May 1, 1992
Detection of a frequent polymorphism in exon 10 of the low-density lipoprotein receptor geneL Warnich, M J Kotze, E Langenhoven, et al.
Molecular and Cellular Probes|June 22, 2005
Analysis of the three common mutations in the CARD15 gene (R702W, G908R and 1007fs) in South African colored patients with inflammatory bowel diseaseM G Zaahl, T Winter, L Warnich, et al.
World Journal of Surgery|May 19, 2016
Postmenopausal Breast Cancer, Aromatase Inhibitors, and Bone Health: What the Surgeon Should KnowK J Baatjes, J P Apffelstaedt, M J Kotze, et al.
Anti-Cancer Agents in Medicinal Chemistry|April 14, 2017
Pharmacogenetics of Aromatase Inhibitors in Endocrine Responsive Breast Cancer: Lessons Learnt from Tamoxifen and CYP2D6 GenotypingK J Baatjes, M Conradie, J P Apffelstaedt, et al.
Human Molecular Genetics|July 13, 1999
Spectrum of mutations in the HFE gene implicated in haemochromatosis and porphyriaJ N de Villiers, R Hillermann, L Loubser, et al.
Pageof 9

Showing results (1-10 of 82) with videos related to

Sort By:
Pageof 9
Blood Cells, Molecules & Diseases|November 27, 1999
Significance of linkage disequilibrium between mutation C282Y and a MseI polymorphism in population screening and DNA diagnosis of hemochromatosisJ N de Villiers, M J Kotze
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|February 16, 2002
Clinical versus molecular diagnosis of heterozygous familial hypercholesterolaemia in the diverse South African populationJ Vergotine, R Thiart, M J Kotze
Molecular and Cellular Probes|February 1, 1995
Screening South African familial adenomatous polyposis families for the five-nucleotide deletion at codon 1309 of the APC geneJ J Grobbelaar, C J Oosthuizen, M J Kotze
Human Genetics|August 1, 1989
Multiple mutations underlying familial hypercholesterolemia in the South African populationH E Henderson, M J Kotze, G M Berger
SADJ : Journal of the South African Dental Association = Tydskrif Van Die Suid-Afrikaanse Tandheelkundige Vereniging|November 29, 2012
A radiological method to evaluate alveolar bone regeneration in the Chacma baboon (Papio ursinus)M J Kotze, K W Bütow, H F Kotze
Human Genetics|May 1, 1992
Detection of a frequent polymorphism in exon 10 of the low-density lipoprotein receptor geneL Warnich, M J Kotze, E Langenhoven, et al.
Molecular and Cellular Probes|June 22, 2005
Analysis of the three common mutations in the CARD15 gene (R702W, G908R and 1007fs) in South African colored patients with inflammatory bowel diseaseM G Zaahl, T Winter, L Warnich, et al.
World Journal of Surgery|May 19, 2016
Postmenopausal Breast Cancer, Aromatase Inhibitors, and Bone Health: What the Surgeon Should KnowK J Baatjes, J P Apffelstaedt, M J Kotze, et al.
Anti-Cancer Agents in Medicinal Chemistry|April 14, 2017
Pharmacogenetics of Aromatase Inhibitors in Endocrine Responsive Breast Cancer: Lessons Learnt from Tamoxifen and CYP2D6 GenotypingK J Baatjes, M Conradie, J P Apffelstaedt, et al.
Human Molecular Genetics|July 13, 1999
Spectrum of mutations in the HFE gene implicated in haemochromatosis and porphyriaJ N de Villiers, R Hillermann, L Loubser, et al.
Pageof 9