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Human Genetics
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June 9, 1978
The HLA system and leprosy in Thailand
J Greiner, E Schleiermacher, T Smith, et al.
Human Genetics
|
June 27, 1978
Genetic polymorphism of the second component of human complement (C2): presentation of a modified typing technique and data on C2 phenotype distribution, linkage genetics, and haplotype associations a Norwegian family material
B Olaisen, P Teisberg, T Gedde-Dahl, et al.
Human Genetics
|
June 27, 1978
Patau's syndrome and 13q21q translocation
A Pérez-Castillo, J A Abrisqueta
Human Genetics
|
June 27, 1978
Terminal deletion of the long arm of chromosome 1 in a malformed newborn
E Kessel, R A Pfeiffer, W Blanke, et al.
Human Genetics
|
June 27, 1978
Ring chromosome 3 in a retarded boy
R Witkowski, E Ullrich, U Piede
Human Genetics
|
January 1, 1984
Characterization of the distribution of sister chromatid exchange frequencies: implications for research design
B Hirsch, M McGue, J Cervenka
Human Genetics
|
January 1, 1984
Meiotic studies in two infertile males with autosomal translocations
M Mićić, S Mićić
Human Genetics
|
January 1, 1984
Cytogenetic studies in spontaneous abortuses
T Andrews, W Dunlop, D F Roberts
Human Genetics
|
January 1, 1984
Isoelectric focusing studies of human red cell esterase D: evidence for polymorphic occurrence of a new allele EsD7 in Japanese
I Nishigaki, T Itoh
Human Genetics
|
January 1, 1983
Genetic control of platelet glutaminase: a twin study
S Sahai, F Vogel
Page
of 1,127
Search research articles
Search
Showing results (421-430 of 11,264) with videos related to
Sort By:
Page
of 1,127
Human Genetics
|
June 9, 1978
The HLA system and leprosy in Thailand
J Greiner, E Schleiermacher, T Smith, et al.
Human Genetics
|
June 27, 1978
Genetic polymorphism of the second component of human complement (C2): presentation of a modified typing technique and data on C2 phenotype distribution, linkage genetics, and haplotype associations a Norwegian family material
B Olaisen, P Teisberg, T Gedde-Dahl, et al.
Human Genetics
|
June 27, 1978
Patau's syndrome and 13q21q translocation
A Pérez-Castillo, J A Abrisqueta
Human Genetics
|
June 27, 1978
Terminal deletion of the long arm of chromosome 1 in a malformed newborn
E Kessel, R A Pfeiffer, W Blanke, et al.
Human Genetics
|
June 27, 1978
Ring chromosome 3 in a retarded boy
R Witkowski, E Ullrich, U Piede
Human Genetics
|
January 1, 1984
Characterization of the distribution of sister chromatid exchange frequencies: implications for research design
B Hirsch, M McGue, J Cervenka
Human Genetics
|
January 1, 1984
Meiotic studies in two infertile males with autosomal translocations
M Mićić, S Mićić
Human Genetics
|
January 1, 1984
Cytogenetic studies in spontaneous abortuses
T Andrews, W Dunlop, D F Roberts
Human Genetics
|
January 1, 1984
Isoelectric focusing studies of human red cell esterase D: evidence for polymorphic occurrence of a new allele EsD7 in Japanese
I Nishigaki, T Itoh
Human Genetics
|
January 1, 1983
Genetic control of platelet glutaminase: a twin study
S Sahai, F Vogel
Page
of 1,127