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Showing results (331-340 of 2,905) with videos related to
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Human Heredity
|
January 1, 1984
Alpha-1-antitrypsin types and pulmonary disease among employees at a sulphite pulp factory in northern Sweden
N Stjernberg, G Beckman, L Beckman, et al.
Human Heredity
|
March 1, 1995
Refined localization of human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to 3p22
F Ottone, E Raimondi, M Rocchi, et al.
Human Heredity
|
November 1, 1994
An association study between schizophrenia and the dopamine receptor genes DRD3 and DRD4 using haplotype relative risk
F Macciardi, M Verga, J L Kennedy, et al.
Human Heredity
|
January 1, 1970
Frequency of colour blindness among the Jats
P K Chattopadhyay
Human Heredity
|
January 1, 1971
Genetic structure of the population of Valparaiso. V. ABO blood groups, color vision deficiency and their relationship to other variables
J Pinto-Cisternas, H Figueroa, B Lazo, et al.
Human Heredity
|
January 1, 1976
Alpha-fetoprotein concentration in cord blood from twins and from a set of quadruplets--a case of superfetatio?
B Norgaard-Pedersen, J Moller, D Trolle, et al.
Human Heredity
|
January 1, 1981
Hitchhiking and linkage disequilibrium between hemoglobin S and nearby restriction sites
D S Straus, C E Taylor
Human Heredity
|
January 1, 1982
Polymorphism of human galactose-1-phosphate uridyl transferase
J C Mulley
Human Heredity
|
January 1, 1981
Human genetics in Burma
H Kyu, A Thu, P J Cook
Human Heredity
|
September 1, 1994
Analysis of factor VIII gene polymorphisms in Brazilian blacks reveals further differences in the black population
W A da Silva Júnior, M S Figueiredo
Page
of 291
Search research articles
Search
Showing results (331-340 of 2,905) with videos related to
Sort By:
Page
of 291
Human Heredity
|
January 1, 1984
Alpha-1-antitrypsin types and pulmonary disease among employees at a sulphite pulp factory in northern Sweden
N Stjernberg, G Beckman, L Beckman, et al.
Human Heredity
|
March 1, 1995
Refined localization of human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to 3p22
F Ottone, E Raimondi, M Rocchi, et al.
Human Heredity
|
November 1, 1994
An association study between schizophrenia and the dopamine receptor genes DRD3 and DRD4 using haplotype relative risk
F Macciardi, M Verga, J L Kennedy, et al.
Human Heredity
|
January 1, 1970
Frequency of colour blindness among the Jats
P K Chattopadhyay
Human Heredity
|
January 1, 1971
Genetic structure of the population of Valparaiso. V. ABO blood groups, color vision deficiency and their relationship to other variables
J Pinto-Cisternas, H Figueroa, B Lazo, et al.
Human Heredity
|
January 1, 1976
Alpha-fetoprotein concentration in cord blood from twins and from a set of quadruplets--a case of superfetatio?
B Norgaard-Pedersen, J Moller, D Trolle, et al.
Human Heredity
|
January 1, 1981
Hitchhiking and linkage disequilibrium between hemoglobin S and nearby restriction sites
D S Straus, C E Taylor
Human Heredity
|
January 1, 1982
Polymorphism of human galactose-1-phosphate uridyl transferase
J C Mulley
Human Heredity
|
January 1, 1981
Human genetics in Burma
H Kyu, A Thu, P J Cook
Human Heredity
|
September 1, 1994
Analysis of factor VIII gene polymorphisms in Brazilian blacks reveals further differences in the black population
W A da Silva Júnior, M S Figueiredo
Page
of 291