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British Journal of Haematology
|
May 8, 1999
A second mutation in the methylenetetrahydrofolate reductase gene and the risk of venous thrombotic disease
R F Franco, V Morelli, D Lourenço, et al.
American Journal of Human Biology : the Official Journal of the Human Biology Council
|
September 5, 2001
Heterogeneity of Y chromosome markers among Brazilian Amerindians
Antonio C.R. Vallinoto, Izaura M.V. Cayres-Vallinoto, Ândrea K.C. Ribeiro Dos Santos ÂK, et al.
Human Biology
|
April 1, 1997
Evolutionary and anthropological implications of mitochondrial DNA variation in African Brazilian populations
M C Bortolini, M A Zago, F M Salzano, et al.
Haematologica
|
February 27, 2001
Rearrangements of the beta-globin gene cluster in apparently typical betaS haplotypes
M A Zago, W A Silva, S Gualandro, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
October 16, 2007
miRNA expression profiles in chronic lymphocytic and acute lymphocytic leukemia
D L Zanette, F Rivadavia, G A Molfetta, et al.
Hepatology (Baltimore, Md.)
|
April 27, 2011
Constitutional telomerase mutations are genetic risk factors for cirrhosis
Rodrigo T Calado, Jennifer Brudno, Paulomi Mehta, et al.
Hemoglobin
|
December 3, 2003
A different molecular pattern of beta-thalassemia mutations in northeast Brazil
Aderson S Araújo, l Wilson A Júnior Silva, Silvana A C Leão, et al.
Haematologica
|
September 2, 2004
Lack of mutations in the human telomerase RNA component (hTERC) gene in Fanconi's anemia
Rodrigo T Calado, Maria-Carolina Pintão, Vanderson Rocha, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
April 11, 2002
Hyperhomocysteinemia increases the risk of venous thrombosis independent of the C677T mutation of the methylenetetrahydrofolate reductase gene in selected Brazilian patients
V M Morelli, D M Lourenço, V D'Almeida, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
November 2, 2004
Hereditary motor and autonomic neuronopathy 1 maps to chromosome 20q13.2-13.3
W Marques, M B Davis, P M Abou-Sleiman, et al.
Page
of 19
Search research articles
Search
Showing results (121-130 of 187) with videos related to
Sort By:
Page
of 19
British Journal of Haematology
|
May 8, 1999
A second mutation in the methylenetetrahydrofolate reductase gene and the risk of venous thrombotic disease
R F Franco, V Morelli, D Lourenço, et al.
American Journal of Human Biology : the Official Journal of the Human Biology Council
|
September 5, 2001
Heterogeneity of Y chromosome markers among Brazilian Amerindians
Antonio C.R. Vallinoto, Izaura M.V. Cayres-Vallinoto, Ândrea K.C. Ribeiro Dos Santos ÂK, et al.
Human Biology
|
April 1, 1997
Evolutionary and anthropological implications of mitochondrial DNA variation in African Brazilian populations
M C Bortolini, M A Zago, F M Salzano, et al.
Haematologica
|
February 27, 2001
Rearrangements of the beta-globin gene cluster in apparently typical betaS haplotypes
M A Zago, W A Silva, S Gualandro, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
October 16, 2007
miRNA expression profiles in chronic lymphocytic and acute lymphocytic leukemia
D L Zanette, F Rivadavia, G A Molfetta, et al.
Hepatology (Baltimore, Md.)
|
April 27, 2011
Constitutional telomerase mutations are genetic risk factors for cirrhosis
Rodrigo T Calado, Jennifer Brudno, Paulomi Mehta, et al.
Hemoglobin
|
December 3, 2003
A different molecular pattern of beta-thalassemia mutations in northeast Brazil
Aderson S Araújo, l Wilson A Júnior Silva, Silvana A C Leão, et al.
Haematologica
|
September 2, 2004
Lack of mutations in the human telomerase RNA component (hTERC) gene in Fanconi's anemia
Rodrigo T Calado, Maria-Carolina Pintão, Vanderson Rocha, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
April 11, 2002
Hyperhomocysteinemia increases the risk of venous thrombosis independent of the C677T mutation of the methylenetetrahydrofolate reductase gene in selected Brazilian patients
V M Morelli, D M Lourenço, V D'Almeida, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
November 2, 2004
Hereditary motor and autonomic neuronopathy 1 maps to chromosome 20q13.2-13.3
W Marques, M B Davis, P M Abou-Sleiman, et al.
Page
of 19