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EVERSOLECIRE P
SPRUCK CH
HUSTAD CM
COETZEE GA
GONZALES FA
JONES PA
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RAAL D
SEFTEL H
PILCHER G
COETZEE GA
VANDERWESTHUYZEN DR
Citation: Dc. Rubinsztein et al., CHARACTERIZATION OF 6 PATIENTS WHO ARE DOUBLE HETEROZYGOTES FOR FAMILIAL HYPERCHOLESTEROLEMIA AND FAMILIAL DEFECTIVE APOLIPOPROTEIN B-100, Journal of Medical Genetics, 31(2), 1994, pp. 172-172
Authors:
KOTZE MJ
DEVILLIERS WJS
STEYN K
KRIEK JA
MARAIS AD
LANGENHOVEN E
HERBERT JS
VANROGGEN JFG
VANDERWESTHUYZEN DR
COETZEE GA
Citation: Mj. Kotze et al., PHENOTYPIC VARIATION AMONG FAMILIAL HYPERCHOLESTEROLEMICS HETEROZYGOUS FOR EITHER ONE OF 2 AFRIKANER FOUNDER LDL RECEPTOR MUTATIONS, Arteriosclerosis and thrombosis, 13(10), 1993, pp. 1460-1468
Citation: Ad. Marais et al., DYSLIPOPROTEINEMIA - AN OVERVIEW WITH SPECIAL REFERENCE TO FAMILIAL HYPERCHOLESTEROLEMIA, Transfusion science, 14(3), 1993, pp. 223-237
Authors:
RUBINSZTEIN DC
JIALAL I
LEITERSDORF E
COETZEE GA
VANDERWESTHUYZEN DR
Citation: Dc. Rubinsztein et al., IDENTIFICATION OF 2 NEW LDL-RECEPTOR MUTATIONS CAUSING HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA IN A SOUTH-AFRICAN OF INDIAN ORIGIN, Biochimica et biophysica acta, 1182(1), 1993, pp. 75-82