Retief AE - Search Results

1

The CEPH consortium linkage map of human chromosome 13.

Bowcock AM, Gerken SC, Barnes RI, Shiang R, Jabs EW, Warren AC, Antonarakis S, Retief AE, Vergnaud G, Leppert M, et al. Bowcock AM, et al. Among authors: retief ae. Genomics. 1993 May;16(2):486-96. doi: 10.1006/geno.1993.1215. Genomics. 1993. PMID: 8314586

2

Linkage map of eight human chromosome 11q markers, including DRD2, spanning 60 cM.

Gelernter J, Pakstis AJ, Grandy D, Litt M, Retief AE, Kennedy JL, Hing-Loh A, Schoolfield G, Civelli O, Kidd KK. Gelernter J, et al. Among authors: retief ae. Cytogenet Cell Genet. 1992;60(1):26-8. doi: 10.1159/000133287. Cytogenet Cell Genet. 1992. PMID: 1349858

3

Mapping of the variegate porphyria (VP) gene: contradictory evidence for linkage between VP and microsatellite markers at chromosome 14q32.

Warnich L, Meissner PN, Hift RJ, Louw JH, van Heerden CJ, Retief AE. Warnich L, et al. Among authors: retief ae. Hum Genet. 1996 May;97(5):690-2. doi: 10.1007/BF02281885. Hum Genet. 1996. PMID: 8655155

4

Dinucleotide repeat polymorphism at the D5S99 locus on chromosome 5q33-34.

Groenewald IM, Warnich L, Retief AE. Groenewald IM, et al. Among authors: retief ae. Hum Genet. 1995 Oct;96(4):497-9. doi: 10.1007/BF00191818. Hum Genet. 1995. PMID: 7557982

5

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: retief ae. Hum Mol Genet. 1996 Jul;5(7):981-4. doi: 10.1093/hmg/5.7.981. Hum Mol Genet. 1996. PMID: 8817334

6

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. Among authors: retief ae. Ann Hum Genet. 1991 May;55(2):115-21. doi: 10.1111/j.1469-1809.1991.tb00404.x. Ann Hum Genet. 1991. PMID: 1952806

7

Highly informative dinucleotide repeat polymorphism at the D11S29 locus on chromosome 11q23.

Warnich L, Groenewald I, Theart L, Retief AE. Warnich L, et al. Among authors: retief ae. Hum Genet. 1992 May;89(3):357-9. doi: 10.1007/BF00220560. Hum Genet. 1992. PMID: 1601428

8

Molecular analysis reveals a high mutation frequency in the first untranslated exon of the PPOX gene and largely excludes variegate porphyria in a subset of clinically affected Afrikaner families.

Kotze MJ, De Villiers JN, Groenewald JZ, Rooney RN, Loubser O, Thiart R, Oosthuizen CJ, van Niekerk MM, Groenewald IM, Retief AE, Warnich L. Kotze MJ, et al. Among authors: retief ae. Mol Cell Probes. 1998 Oct;12(5):293-300. doi: 10.1006/mcpr.1998.0188. Mol Cell Probes. 1998. PMID: 9778454

9

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: retief ae. Hum Genet. 1992 May;89(3):362. doi: 10.1007/BF00220563. Hum Genet. 1992. PMID: 1601429

10

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. Among authors: retief ae. 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.

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