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A E Retief

Showing results (61-70 of 67) with videos related to

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Nucleic Acids Research|February 25, 1986
An anonymous human single copy genomic clone, D11S29 (L7) at 11q23, identifies a moderately frequent RFLPL Warnich, M J Kotze, A E Retief, et al.
Nucleic Acids Research|August 26, 1986
An anonymous human single copy genomic clone (D8S5) (TL11) on chromosome 8 identifies a moderately frequent RFLPE Dietzsch, A E Retief, L Warnich, et al.
Journal of Medical Genetics|December 1, 1987
Haplotype associations of three DNA polymorphisms at the human low density lipoprotein receptor gene locus in familial hypercholesterolaemiaM J Kotze, E Langenhoven, A E Retief, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Linkage map of eight human chromosome 11q markers, including DRD2, spanning 60 cMJ Gelernter, A J Pakstis, D Grandy, et al.
Genomics|May 1, 1993
The CEPH consortium linkage map of human chromosome 13A M Bowcock, S C Gerken, R I Barnes, et al.
Molecular and Cellular Probes|October 21, 1998
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 familiesM J Kotze, J N De Villiers, J Z Groenewald, et al.
Human Molecular Genetics|July 1, 1996
Identification of three mutations and associated haplotypes in the protoporphyrinogen oxidase gene in South African families with variegate porphyriaL Warnich, M J Kotze, I M Groenewald, et al.
Pageof 7

Showing results (61-70 of 67) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 67 results.
Nucleic Acids Research|February 25, 1986
An anonymous human single copy genomic clone, D11S29 (L7) at 11q23, identifies a moderately frequent RFLPL Warnich, M J Kotze, A E Retief, et al.
Nucleic Acids Research|August 26, 1986
An anonymous human single copy genomic clone (D8S5) (TL11) on chromosome 8 identifies a moderately frequent RFLPE Dietzsch, A E Retief, L Warnich, et al.
Journal of Medical Genetics|December 1, 1987
Haplotype associations of three DNA polymorphisms at the human low density lipoprotein receptor gene locus in familial hypercholesterolaemiaM J Kotze, E Langenhoven, A E Retief, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Linkage map of eight human chromosome 11q markers, including DRD2, spanning 60 cMJ Gelernter, A J Pakstis, D Grandy, et al.
Genomics|May 1, 1993
The CEPH consortium linkage map of human chromosome 13A M Bowcock, S C Gerken, R I Barnes, et al.
Molecular and Cellular Probes|October 21, 1998
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 familiesM J Kotze, J N De Villiers, J Z Groenewald, et al.
Human Molecular Genetics|July 1, 1996
Identification of three mutations and associated haplotypes in the protoporphyrinogen oxidase gene in South African families with variegate porphyriaL Warnich, M J Kotze, I M Groenewald, et al.
Pageof 7