Search research articles
Contact Us
Filters
Showing results (61-70 of 67) with videos related to
Page
of 7
Sort By:
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 RFLP
L 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 RFLP
E 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 hypercholesterolaemia
M 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 cM
J Gelernter, A J Pakstis, D Grandy, et al.
Genomics
|
May 1, 1993
The CEPH consortium linkage map of human chromosome 13
A 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 families
M 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 porphyria
L Warnich, M J Kotze, I M Groenewald, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 67) with videos related to
Sort By:
Page
of 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 RFLP
L 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 RFLP
E 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 hypercholesterolaemia
M 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 cM
J Gelernter, A J Pakstis, D Grandy, et al.
Genomics
|
May 1, 1993
The CEPH consortium linkage map of human chromosome 13
A 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 families
M 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 porphyria
L Warnich, M J Kotze, I M Groenewald, et al.
Page
of 7