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A E Retief

Showing results (21-30 of 67) with videos related to

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Journal of Medical Genetics|July 1, 1989
Ring chromosome 15 in a patient with features of Fryns' syndromeG de Jong, R A Rossouw, A E Retief
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|August 5, 1989
Identification of gene mutations allows for the molecular diagnosis of familial hypercholesterolemiaA E Retief, M J Kotze, C J Oosthuizen
Nucleic Acids Research|January 12, 1987
A RFLP associated with the low-density lipoprotein receptor gene (LDLR)M J Kotze, E Langenhoven, E Dietzsch, et al.
Human Genetics|May 1, 1992
Detection of a frequent polymorphism in exon 10 of the low-density lipoprotein receptor geneL Warnich, M J Kotze, E Langenhoven, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|March 29, 1975
[Problems with reference to genetic counseling in arthrogryposis multiplex congenits]G S Gericke, A E Retief, W A Van Niekerk
Cytogenetics and Cell Genetics|January 1, 1984
Regional localization of alpha-galactosidase (GLA) to Xpter----q22, hexosaminidase B (HEXB) to 5q13----qter, and arylsulfatase B (ARSB) to 5pter----q13M F Fox, D L DuToit, L Warnich, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|March 15, 1975
Letter: Ehler-Danlos syndromeG S Gericke, F Maritz, A E Retief, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|July 19, 1986
A DNA polymorphism in the human low-density lipoprotein receptor geneM J Kotze, A E Retief, P A Brink, et al.
Nucleic Acids Research|January 11, 1989
Anonymous DNA segment H33 [D6S42] on chromosome 6 associated with 2 RFLPsL Warnich, E Dietzsch, D A Heyns, et al.
Annals of Human Genetics|May 1, 1991
The molecular basis and diagnosis of familial hypercholesterolaemia in South African AfrikanersM J Kotze, E Langenhoven, L Warnich, et al.
Pageof 7

Showing results (21-30 of 67) with videos related to

Sort By:
Pageof 7
Journal of Medical Genetics|July 1, 1989
Ring chromosome 15 in a patient with features of Fryns' syndromeG de Jong, R A Rossouw, A E Retief
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|August 5, 1989
Identification of gene mutations allows for the molecular diagnosis of familial hypercholesterolemiaA E Retief, M J Kotze, C J Oosthuizen
Nucleic Acids Research|January 12, 1987
A RFLP associated with the low-density lipoprotein receptor gene (LDLR)M J Kotze, E Langenhoven, E Dietzsch, et al.
Human Genetics|May 1, 1992
Detection of a frequent polymorphism in exon 10 of the low-density lipoprotein receptor geneL Warnich, M J Kotze, E Langenhoven, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|March 29, 1975
[Problems with reference to genetic counseling in arthrogryposis multiplex congenits]G S Gericke, A E Retief, W A Van Niekerk
Cytogenetics and Cell Genetics|January 1, 1984
Regional localization of alpha-galactosidase (GLA) to Xpter----q22, hexosaminidase B (HEXB) to 5q13----qter, and arylsulfatase B (ARSB) to 5pter----q13M F Fox, D L DuToit, L Warnich, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|March 15, 1975
Letter: Ehler-Danlos syndromeG S Gericke, F Maritz, A E Retief, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|July 19, 1986
A DNA polymorphism in the human low-density lipoprotein receptor geneM J Kotze, A E Retief, P A Brink, et al.
Nucleic Acids Research|January 11, 1989
Anonymous DNA segment H33 [D6S42] on chromosome 6 associated with 2 RFLPsL Warnich, E Dietzsch, D A Heyns, et al.
Annals of Human Genetics|May 1, 1991
The molecular basis and diagnosis of familial hypercholesterolaemia in South African AfrikanersM J Kotze, E Langenhoven, L Warnich, et al.
Pageof 7