Charlotte L. Scholtz

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

G. Gebhardt, Charlotte L. Scholtz, Renate Hillermann et al. · European Journal of Obstetrics & Gynecology and Reproductive Biology · 2001 · 41 citations

Developmental Biology, Placental Development, Genetic Disorder +13

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

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

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

Genetic Testing, Cardiovascular Disease, South African Patients +9

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

Lipid Disorder, Allelic Variant, Heterozygous Familial Hypercholesterolemia +8