The prenatal development of the optic fissure in colobomatous microphthalmia
Hero, I, Farjah, M, Scholtz, CL
Published in Investigative ophthalmology & visual science (01.08.1991)
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Published in Investigative ophthalmology & visual science (01.08.1991)
Journal Article
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 Hypercholesterolaemia
Scholtz, Charlotte L., Peeters, Armand V., Hoogendijk, Christiaan F., Thiart, Rochelle, de Villiers, J.N.P., Hillermann, Renate, Liu, Jingwen, Marais, A. David, Kotze, Maritha J.
Published in Human molecular genetics (01.10.1999)
Published in Human molecular genetics (01.10.1999)
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Journal Article
Predominance of a 6 bp deletion in exon 2 of the LDL receptor gene in Africans with familial hypercholesterolaemia
Thiart, Rochelle, Scholtz, Charlotte L, Vergotine, Joseph, Hoogendijk, Christiaan F, de Villiers, J Nico P, Nissen, Henrik, Brusgaard, Klaus, Gaffney, Dairena, Hoffs, Michael S, Vermaak, W J Hayward, Kotze, Maritha J
Published in Journal of medical genetics (01.07.2000)
Published in Journal of medical genetics (01.07.2000)
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Journal Article
Founder mutations in the LDL receptor gene contribute significantly to the familial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry
Loubser, Odell, Marais, A David, Kotze2, Maritha J, Godenir, Nicole, Thiart2, Rochelle, Scholtz2, Charlotte L, De Villiers2, J Nico P, Hillermann2, Renate, Firth, Jean C, Weich, Hellmuth Fh, Maritz, Frans, Jones2, Sheena, Van Der Westhuyzen, Deneys R
Published in Clinical genetics (01.05.1999)
Published in Clinical genetics (01.05.1999)
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Journal Article
Omnipause neurons in two cases of opsoclonus associated with oat cell carcinoma of the lung
Ridley, A, Kennard, C, Scholtz, C L, Büttner-Ennever, J A, Summers, B, Turnbull, A
Published in Brain (London, England : 1878) (01.12.1987)
Published in Brain (London, England : 1878) (01.12.1987)
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Journal Article
Allelic variation in the promoter region of the LDL receptor gene: analysis of an African-specific variant in the FP2 cis-acting regulatory element
Hoogendijk, C.F, Scholtz, C.L, Pimstone, S.M, Ehrenborg, E, Kastelein, J.J P, Defesche, J.C, Thiart, R, du Plessis, L, de Villiers, J.N.P, Zaahl, M.G, Delport, R, Rubinsztein, D.C, Raffel, L.J, Grim, C.E, Mediene-Benchekor, S, Amouyel, P, Brousseau, T, Steyn, K, Lombard, C.J, Hayden, M.R, Kotze, M.J
Published in Molecular and cellular probes (01.08.2003)
Published in Molecular and cellular probes (01.08.2003)
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Journal Article
A double mutant LDL receptor allele in a Cypriot family with heterozygous familial hypercholesterolemia
KOTZE, M. J, DE VILLIERS, J. N. P, LOUBSER, O, THIART, R, SCHOLTZ, C. L, RAAL, F. J
Published in Human genetics (01.07.1997)
Published in Human genetics (01.07.1997)
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Journal Article
The glial reaction in closed head injuries
Crooks, D A, Scholtz, C L, Vowles, G, Greenwald, S, Evans, S
Published in Neuropathology and applied neurobiology (01.10.1991)
Published in Neuropathology and applied neurobiology (01.10.1991)
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Journal Article
Familial adenomatous polyposis coli in South Africa : Molecular basis and diagnosis
GROBBELAAR, J. J, FORTUIN, R, SCHOLTZ, C. L, ZIKIND, A, LANGENHOVEN, E, WYLLIE, A. H, BUBB, V. J, KOTZE, M. J
Published in South African medical journal (01.07.2000)
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Published in South African medical journal (01.07.2000)
Journal Article
Congenital amaurotic idiocy--a pathological, histochemical, biochemical and ultrastructural study
Humphreys, S, Lake, B D, Scholtz, C L
Published in Neuropathology and applied neurobiology (01.11.1985)
Published in Neuropathology and applied neurobiology (01.11.1985)
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Journal Article
Neurofibrillary neuronal degeneration in dialysis dementia: a feature of aluminum toxicity
Scholtz, C L, Swash, M, Gray, A, Kogeorgos, J, Marsh, F
Published in Clinical neuropathology (01.05.1987)
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Published in Clinical neuropathology (01.05.1987)
Journal Article
Combined heterozygosity for methylenetetrahydrofolate reductase (MTHFR) mutations C677T and A1298C is associated with abruptio placentae but not with intrauterine growth restriction
Gebhardt, Gabriël S., Scholtz, Charlotte L., Hillermann, Renate, Odendaal, Hein J.
Published in European journal of obstetrics & gynecology and reproductive biology (01.08.2001)
Published in European journal of obstetrics & gynecology and reproductive biology (01.08.2001)
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Journal Article
Squamous cell carcinoma of the middle ear. A 25-year retrospective study
Kenyon, G S, Marks, P V, Scholtz, C L, Dhillon, R
Published in Annals of otology, rhinology & laryngology (01.05.1985)
Published in Annals of otology, rhinology & laryngology (01.05.1985)
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