Charlotte L. Scholtz

Combined heterozygosity for methylenetetrahydrofolate reductase (MTHFR) mutations C677T and A1298C is associated with abruptio placentae but not with intrauterine growth restriction

Charlotte L. Scholtz, Renate Hillermann, Hein J. Odendaal · European Journal of Obstetrics & Gynecology and Reproductive Biology · 2001 · 41 citations

Life Sciences, Genetics, Molecular Genetics +14

Founder mutations in the LDL receptor gene contribute significantly to the familial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry

Odell Loubser, A. David Marais, Maritha J. Kotze et al. · Clinical Genetics · 1999 · 33 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Analysis of two mutations in the MTHFR gene associated with mild hyperhomocysteinaemia--heterogeneous distribution in the South African population.

Charlotte L. Scholtz, Hein J. Odendaal, Rochelle Thiart et al. · PubMed · 2002 · 20 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Simultaneous Detection of Multiple Familial Hypercholesterolemia Mutations Facilitates an Improved Diagnostic Service in South African Patients at High Risk of Cardiovascular Disease

Maritha J. Kotze, Gernot Kriegshäuser, Rochelle Thiart et al. · Molecular Diagnosis · 2003 · 17 citations

Medicine, Cardiology, Genetics +17

A double mutant LDL receptor allele in a Cypriot family with heterozygous familial hypercholesterolemia

Maritha J. Kotze, J. Nico P. de Villiers, Odell Loubser et al. · Human Genetics · 1997 · 15 citations

Life Sciences, Genetics, Molecular Genetics +13