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Journal of Medical Genetics
|
October 1, 1986
Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2)
J Brusnický, K M van Heerden, G de Jong, et al.
Nucleic Acids Research
|
June 11, 1990
An anonymous DNA probe H35 (D9S41) on chromosome 9 detects a TaqI polymorphism
L Warnich, E Dietzsch, J Brusnický, et al.
Nucleic Acids Research
|
March 11, 1987
Frequent RFLP recognised by an anonymous sequence localised to 11q13 - q14 [D11S.3.7.(E79)]
E Dietzsch, A E Retief, J Fricke, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
June 7, 1975
Clinical and cytogenetic aspects of the 21 deletion syndrome
G S Gericke, M F Steyn, A E Retief, et al.
Human Genetics
|
January 1, 1984
No marker (X) syndrome in autistic children
P A Venter, J Op't Hof, D J Coetzee, et al.
Journal of Medical Genetics
|
April 1, 1989
Haplotypes identified by 10 DNA restriction fragment length polymorphisms at the human low density lipoprotein receptor gene locus
M J Kotze, E Langenhoven, A E Retief, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
January 8, 1983
A 3-year cytogenetic survey of 9 661 patients in South Africa
A E Retief, R Bernstein, H J Grace, et al.
International Journal of Fertility
|
January 1, 1975
Oligozoospermia: a seven-year survey of the incidence, chromosomal aberrations, treatment and pregnancy rate
J A van Zyl, R Menkveld, T J van Kotze, et al.
Human Genetics
|
January 1, 1984
Chromosome studies in 496 infertile males with a sperm count below 10 million/ml
A E Retief, J A Van Zyl, R Menkveld, et al.
Nucleic Acids Research
|
January 26, 1987
Isolation of an anonymous single copy probe D4S66 (E24) from chromosome 4 associated with a three allele RFLP
E Dietzsch, A E Retief, J Fricke, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 67) with videos related to
Sort By:
Page
of 7
Journal of Medical Genetics
|
October 1, 1986
Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2)
J Brusnický, K M van Heerden, G de Jong, et al.
Nucleic Acids Research
|
June 11, 1990
An anonymous DNA probe H35 (D9S41) on chromosome 9 detects a TaqI polymorphism
L Warnich, E Dietzsch, J Brusnický, et al.
Nucleic Acids Research
|
March 11, 1987
Frequent RFLP recognised by an anonymous sequence localised to 11q13 - q14 [D11S.3.7.(E79)]
E Dietzsch, A E Retief, J Fricke, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
June 7, 1975
Clinical and cytogenetic aspects of the 21 deletion syndrome
G S Gericke, M F Steyn, A E Retief, et al.
Human Genetics
|
January 1, 1984
No marker (X) syndrome in autistic children
P A Venter, J Op't Hof, D J Coetzee, et al.
Journal of Medical Genetics
|
April 1, 1989
Haplotypes identified by 10 DNA restriction fragment length polymorphisms at the human low density lipoprotein receptor gene locus
M J Kotze, E Langenhoven, A E Retief, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
January 8, 1983
A 3-year cytogenetic survey of 9 661 patients in South Africa
A E Retief, R Bernstein, H J Grace, et al.
International Journal of Fertility
|
January 1, 1975
Oligozoospermia: a seven-year survey of the incidence, chromosomal aberrations, treatment and pregnancy rate
J A van Zyl, R Menkveld, T J van Kotze, et al.
Human Genetics
|
January 1, 1984
Chromosome studies in 496 infertile males with a sperm count below 10 million/ml
A E Retief, J A Van Zyl, R Menkveld, et al.
Nucleic Acids Research
|
January 26, 1987
Isolation of an anonymous single copy probe D4S66 (E24) from chromosome 4 associated with a three allele RFLP
E Dietzsch, A E Retief, J Fricke, et al.
Page
of 7