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L Warnich

Showing results (11-20 of 24) with videos related to

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Journal of Medical Genetics|May 1, 1990
An exon 4 mutation identified in the majority of South African familial hypercholesterolaemicsM J Kotze, L Warnich, E Langenhoven, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|October 21, 1989
Molecular characterisation of a low-frequency mutation in exon 8 of the human low-density lipoprotein receptor geneM J Kotze, E Langenhoven, L Warnich, et al.
Molecular and Cellular Probes|March 12, 2003
Significance of novel endothelin-B receptor gene polymorphisms in Hirschsprung's disease: predominance of a novel variant (561C/T) in patients with co-existing Down's syndromeM G Zaahl, L du Plessis, L Warnich, et al.
Internal Medicine Journal|October 17, 2002
Variegate porphyria in Western Australian Aboriginal patientsE Rossi, C Y B Chin, J P Beilby, et al.
Human Genetics|May 1, 1996
Mapping of the variegate porphyria (VP) gene: contradictory evidence for linkage between VP and microsatellite markers at chromosome 14q32L Warnich, P N Meissner, R J Hift, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|August 7, 2009
Functional analysis of the 5' regulatory region of the 5-aminolevulinate synthase (ALAS1) gene in response to estrogenN du Plessis, M Kimberg, M G Zaahl, et al.
Atherosclerosis|August 23, 1996
Two novel point mutations causing receptor-negative familial hypercholesterolemia in a South African Indian homozygoteE Langenhoven, L Warnich, R Thiart, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|October 21, 1989
The identification of two low-density lipoprotein receptor gene mutations in South African familial hypercholesterolaemiaM J Kotze, E Langenhoven, L Warnich, et al.
Clinical Genetics|March 18, 2004
Molecular diagnosis of hereditary hemochromatosis: application of a newly-developed reverse-hybridization assay in the South African populationM J Kotze, J N P de Villiers, C S H Bouwens, et al.
Molecular and Cellular Probes|August 22, 2001
Single nucleotide polymorphisms of the protoporphyrinogen oxidase gene: inter-population heterogeneity of allelic variationL Warnich, H F Waso, I M Groenewald, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Journal of Medical Genetics|May 1, 1990
An exon 4 mutation identified in the majority of South African familial hypercholesterolaemicsM J Kotze, L Warnich, E Langenhoven, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|October 21, 1989
Molecular characterisation of a low-frequency mutation in exon 8 of the human low-density lipoprotein receptor geneM J Kotze, E Langenhoven, L Warnich, et al.
Molecular and Cellular Probes|March 12, 2003
Significance of novel endothelin-B receptor gene polymorphisms in Hirschsprung's disease: predominance of a novel variant (561C/T) in patients with co-existing Down's syndromeM G Zaahl, L du Plessis, L Warnich, et al.
Internal Medicine Journal|October 17, 2002
Variegate porphyria in Western Australian Aboriginal patientsE Rossi, C Y B Chin, J P Beilby, et al.
Human Genetics|May 1, 1996
Mapping of the variegate porphyria (VP) gene: contradictory evidence for linkage between VP and microsatellite markers at chromosome 14q32L Warnich, P N Meissner, R J Hift, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|August 7, 2009
Functional analysis of the 5' regulatory region of the 5-aminolevulinate synthase (ALAS1) gene in response to estrogenN du Plessis, M Kimberg, M G Zaahl, et al.
Atherosclerosis|August 23, 1996
Two novel point mutations causing receptor-negative familial hypercholesterolemia in a South African Indian homozygoteE Langenhoven, L Warnich, R Thiart, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|October 21, 1989
The identification of two low-density lipoprotein receptor gene mutations in South African familial hypercholesterolaemiaM J Kotze, E Langenhoven, L Warnich, et al.
Clinical Genetics|March 18, 2004
Molecular diagnosis of hereditary hemochromatosis: application of a newly-developed reverse-hybridization assay in the South African populationM J Kotze, J N P de Villiers, C S H Bouwens, et al.
Molecular and Cellular Probes|August 22, 2001
Single nucleotide polymorphisms of the protoporphyrinogen oxidase gene: inter-population heterogeneity of allelic variationL Warnich, H F Waso, I M Groenewald, et al.
Pageof 3