Kotze MJ - Search Results

1

Identification of three mutations and associated haplotypes in the protoporphyrinogen oxidase gene in South African families with variegate porphyria.

Warnich L, Kotze MJ, Groenewald IM, Groenewald JZ, van Brakel MG, van Heerden CJ, de Villiers JN, van de Ven WJ, Schoenmakers EF, Taketani S, Retief AE. Warnich L, et al. Among authors: kotze mj. Hum Mol Genet. 1996 Jul;5(7):981-4. doi: 10.1093/hmg/5.7.981. Hum Mol Genet. 1996. PMID: 8817334

2

DNA screening of hyperlipidemic Afrikaners for familial hypercholesterolemia.

Kotze MJ, Langenhoven E, Kriek JA, Oosthuizen CJ, Retief AE. Kotze MJ, et al. Clin Genet. 1992 Jul;42(1):43-6. doi: 10.1111/j.1399-0004.1992.tb03135.x. Clin Genet. 1992. PMID: 1516226

3

Detection of a frequent polymorphism in exon 10 of the low-density lipoprotein receptor gene.

Warnich L, Kotze MJ, Langenhoven E, Retief AE. Warnich L, et al. Among authors: kotze mj. Hum Genet. 1992 May;89(3):362. doi: 10.1007/BF00220563. Hum Genet. 1992. PMID: 1601429

4

The molecular basis and diagnosis of familial hypercholesterolaemia in South African Afrikaners.

Kotze MJ, Langenhoven E, Warnich L, du Plessis L, Retief AE. Kotze MJ, et al. Ann Hum Genet. 1991 May;55(2):115-21. doi: 10.1111/j.1469-1809.1991.tb00404.x. Ann Hum Genet. 1991. PMID: 1952806

5

An exon 4 mutation identified in the majority of South African familial hypercholesterolaemics.

Kotze MJ, Warnich L, Langenhoven E, du Plessis L, Retief AE. Kotze MJ, et al. J Med Genet. 1990 May;27(5):298-302. doi: 10.1136/jmg.27.5.298. J Med Genet. 1990. PMID: 2352257 Free PMC article.

6

Haplotypes identified by 10 DNA restriction fragment length polymorphisms at the human low density lipoprotein receptor gene locus.

Kotze MJ, Langenhoven E, Retief AE, Seftel HC, Henderson HE, Weich HF. Kotze MJ, et al. J Med Genet. 1989 Apr;26(4):255-9. doi: 10.1136/jmg.26.4.255. J Med Genet. 1989. PMID: 2565980 Free PMC article.

7

Multiple mutations underlying familial hypercholesterolemia in the South African population.

Henderson HE, Kotze MJ, Berger GM. Henderson HE, et al. Among authors: kotze mj. Hum Genet. 1989 Aug;83(1):67-70. doi: 10.1007/BF00274151. Hum Genet. 1989. PMID: 2570020

8

Molecular characterisation of a low-frequency mutation in exon 8 of the human low-density lipoprotein receptor gene.

Kotze MJ, Langenhoven E, Warnich L, Marx MP, Retief AE. Kotze MJ, et al. S Afr Med J. 1989 Oct 21;76(8):402-5. S Afr Med J. 1989. PMID: 2572061

9

Identification of gene mutations allows for the molecular diagnosis of familial hypercholesterolemia.

Retief AE, Kotze MJ, Oosthuizen CJ. Retief AE, et al. Among authors: kotze mj. S Afr Med J. 1989 Aug 5;76(3):121. S Afr Med J. 1989. PMID: 2762943 No abstract available.

10

The identification of two low-density lipoprotein receptor gene mutations in South African familial hypercholesterolaemia.

Kotze MJ, Langenhoven E, Warnich L, du Plessis L, Marx MP, Oosthuizen CJ, Retief AE. Kotze MJ, et al. S Afr Med J. 1989 Oct 21;76(8):399-401. S Afr Med J. 1989. PMID: 2799589

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