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Annals of Human Genetics
|
November 7, 2002
Identification of two SNPs in the 5' flanking region of the ACP1 gene and evaluation of disequilibrium among polymorphic sites
G Faggioni, P Borgiani, N Bottini, et al.
American Journal of Diseases of Children (1960)
|
April 1, 1986
Genetic polymorphism and intrauterine development: the role of maternal PGM and MNSs genotypes
F Gloria-Bottini, N Lucarini, E Bonci, et al.
American Journal of Human Genetics
|
August 1, 1991
Diabetic pregnancy: is there intrauterine selection of ADA polymorphism?
P Borgiani, F Gloria-Bottini, N Lucarini, et al.
International Journal of Immunopathology and Pharmacology
|
March 25, 2009
Role of interleukin-15 receptor alpha polymorphisms in normal weight obese syndrome
L Di Renzo, F Gloria-Bottini, P Saccucci, et al.
Journal of Medical Genetics
|
October 1, 1981
Adenosine deaminase polymorphism. Associations at clinical level suggest a role in cell functions and immune reactions
E Bottini, E Carapella, L Cataldi, et al.
Diabetes Research (Edinburgh, Scotland)
|
August 1, 1987
Foetal macrosomia in diabetic pregnancy. Further data on the association with maternal PGM1 genotype
N Lucarini, G Gerlini, F Gloria-Bottini, et al.
Neurogenetics
|
October 19, 2004
Convulsive disorder and genetic polymorphism. Association of idiopathic generalized epilepsy with haptoglobin polymorphism
P Saccucci, M Verdecchia, A Piciullo, et al.
Cardiology Research and Practice
|
April 30, 2010
Coronary artery disease: a study on the joint role of birth weight, adenosine deaminase, and gender
F Gloria-Bottini, M Banci, P Saccucci, et al.
Early Human Development
|
January 1, 1985
Serum haptoglobin appearance during neonatal period is associated with acid phosphatase (ACP1) phenotype
E Bottini, E Carapella, R Scacchi, et al.
Journal of Medical Genetics
|
June 1, 1983
Intrauterine death: an approach to the analysis of genetic heterogeneity
E Bottini, L Coromaldi, E Carapella, et al.
Page
of 15
Search research articles
Search
Showing results (101-110 of 141) with videos related to
Sort By:
Page
of 15
Annals of Human Genetics
|
November 7, 2002
Identification of two SNPs in the 5' flanking region of the ACP1 gene and evaluation of disequilibrium among polymorphic sites
G Faggioni, P Borgiani, N Bottini, et al.
American Journal of Diseases of Children (1960)
|
April 1, 1986
Genetic polymorphism and intrauterine development: the role of maternal PGM and MNSs genotypes
F Gloria-Bottini, N Lucarini, E Bonci, et al.
American Journal of Human Genetics
|
August 1, 1991
Diabetic pregnancy: is there intrauterine selection of ADA polymorphism?
P Borgiani, F Gloria-Bottini, N Lucarini, et al.
International Journal of Immunopathology and Pharmacology
|
March 25, 2009
Role of interleukin-15 receptor alpha polymorphisms in normal weight obese syndrome
L Di Renzo, F Gloria-Bottini, P Saccucci, et al.
Journal of Medical Genetics
|
October 1, 1981
Adenosine deaminase polymorphism. Associations at clinical level suggest a role in cell functions and immune reactions
E Bottini, E Carapella, L Cataldi, et al.
Diabetes Research (Edinburgh, Scotland)
|
August 1, 1987
Foetal macrosomia in diabetic pregnancy. Further data on the association with maternal PGM1 genotype
N Lucarini, G Gerlini, F Gloria-Bottini, et al.
Neurogenetics
|
October 19, 2004
Convulsive disorder and genetic polymorphism. Association of idiopathic generalized epilepsy with haptoglobin polymorphism
P Saccucci, M Verdecchia, A Piciullo, et al.
Cardiology Research and Practice
|
April 30, 2010
Coronary artery disease: a study on the joint role of birth weight, adenosine deaminase, and gender
F Gloria-Bottini, M Banci, P Saccucci, et al.
Early Human Development
|
January 1, 1985
Serum haptoglobin appearance during neonatal period is associated with acid phosphatase (ACP1) phenotype
E Bottini, E Carapella, R Scacchi, et al.
Journal of Medical Genetics
|
June 1, 1983
Intrauterine death: an approach to the analysis of genetic heterogeneity
E Bottini, L Coromaldi, E Carapella, et al.
Page
of 15