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JNP De Villiers
JNP De Villiers
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Title
Cited by
Cited by
Year
Spectrum of Mutations in the HFE Gene Implicated in Haemochromatosis and Porphyria
JNP de Villiers, R Hillermann, L Loubser, MJ Kotze
Human Molecular Genetics 8 (8), 1517-1522, 1999
1021999
Identification of three mutations and associated haplotypes in the protoporphyrinogen oxidase gene in South African families with variegate porphyria
L Warnich, MJ Kotze, IM Groenewald, JZ Groenewald, MG van Brakel, ...
Human Molecular Genetics 5 (7), 981-984, 1996
981996
The geology of the Richtersveld
J De Villiers, APG Söhnge
Government Printer, 1959
931959
Analysis of the NRAMP1 gene implicated in iron transport: association with multiple sclerosis and age effects
MJ Kotze, JNP de Villiers, RN Rooney, JJ Grobbelaar, EPG Mansvelt, ...
Blood Cells, Molecules, and Diseases 27 (1), 44-53, 2001
862001
The manganese deposits of the Union of South Africa
J De Villiers
Government Printer, 1960
741960
A Reverse-Hybridization Assay for the Rapid and Simultaneous Detection of Nine HFE Gene Mutations
C Oberkanins, A Moritz, JNP de Villiers, MJ Kotze, F Kury
Genetic Testing 4 (2), 121-124, 2000
652000
Efficiency of a closed-coupled solar pasteurization system in treating roof harvested rainwater
PH Dobrowsky, M Carstens, J De Villiers, TE Cloete, W Khan
Science of the Total Environment 536, 206-214, 2015
632015
Founder mutations in the LDL receptor gene contribute significantly to the familial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry
O Loubser, AD Marais, MJ Kotze2, N Godenir, R Thiart2, CL Scholtz2, ...
Clinical genetics 55 (5), 340-345, 1999
431999
CpG hotspot mutations at the LDL receptor locus are a frequent cause of familial hypercholesterolemia among South African Indians
MJ Kotze, O Loubser, R Thiart, JNP de Villiers, E Langenhoven, L Theart, ...
Clinical genetics 51 (6), 394-398, 1997
361997
Earlier Age of Onset of Alzheimer's Disease in Patients with Both the Transferrin C2 and Apolipoprotein E‐ɛ4 Alleles
SJ Van Rensburg, FCV Potocnik, JNP De Villiers, MJ Kotze, JJF Taljaard
Annals of the New York Academy of Sciences 903 (1), 200-203, 2000
322000
Predominance of a 6 bp deletion in exon 2 of the LDL receptor gene in Africans with familial hypercholesterolaemia
R Thiart, CL Scholtz, J Vergotine, CF Hoogendijk, JNP de Villiers, ...
Journal of medical genetics 37 (7), 514-519, 2000
282000
Mutation− 59c→ t in repeat 2 of the LDL receptor promoter: reduction in transcriptional activity and possible allelic interaction in a South African family with familial …
CL Scholtz, AV Peeters, CF Hoogendijk, R Thiart, JNP De Villiers, ...
Human molecular genetics 8 (11), 2025-2030, 1999
281999
Note on the minimum age of certain granites from the Richtersveld area
J De Villiers, AJ Burger
Ann. Geol. Surv. S. Afr. 6, 83-84, 1967
281967
A review of the Cape Orogeny
J De Villiers
Annale. Kaapstad, 1944
281944
Die Nederlandse era aan die Kaap, 1652-1806
J De Villiers
F. Pretorius (red.), Geskiedenis van Suid-Afrika. Van voortye tot vandag, bl …, 2012
262012
Analysis of viral and genetic factors in South African patients with multiple sclerosis
JNP de Villiers, FK Treurnicht, L Warnich, J Carr, SJ van Rensburg, ...
Metabolic brain disease 21, 156-162, 2006
262006
Molecular diagnosis of hereditary hemochromatosis: application of a newly‐developed reverse‐hybridization assay in the South African population
MJ Kotze, JNP De Villiers, CSH Bouwens, L Warnich, MG Zaahl, ...
Clinical genetics 65 (4), 317-321, 2004
252004
Multiple sclerosis, porphyria‐like symptoms, and a history of iron deficiency anemia in a family of Scottish descent
RN Rooney, MJ Kotze, JNP de Villiers, R Hillermann, JA Cohen
American journal of medical genetics 86 (2), 194-196, 1999
231999
Effect of seaweed foliar sprays on fruit quality and mineral nutrition.
J Villiers, WAG Kotze, M Joubert
231983
Extra-uterine pregnancy at or near term-a case report with a review of the literature
JN De Villiers
South African Medical Journal 28 (13), 254-260, 1954
231954
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