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Biotechniques
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May 22, 2004
SNP allele frequency estimation in DNA pools and variance components analysis
Kate Downes, Bryan J Barratt, Pelin Akan, et al.
Cardiovascular Research
|
July 1, 1989
Variable adaptation of molecular mechanisms in relation to the use of autologous striated muscle to augment myocardial function
C W Pattison, D V Cumming, D G Clayton Jones, et al.
Annals of the New York Academy of Sciences
|
January 1, 1985
Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia
S Pang, M S Pollack, M Loo, et al.
Journal of Vascular Surgery
|
December 18, 2001
Determinants of carotid microembolization
J Golledge, R Gibbs, C Irving, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 1, 1985
Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia
S Pang, M S Pollack, M Loo, et al.
The Journal of Pediatrics
|
April 17, 1998
Pulmonary function in hospitalized infants and toddlers with cystic fibrosis
R G Clayton, C E Diaz, N S Bashir, et al.
The Journal of Thoracic and Cardiovascular Surgery
|
November 1, 1991
Aortic counterpulsation for up to 28 days with autologous latissimus dorsi in sheep
C W Pattison, D V Cumming, A Williamson, et al.
Genetic Epidemiology
|
September 14, 2012
Validity of the family-based association test for copy number variant data in the case of non-linear intensity-genotype relationship
Manuela Zanda, Suna Onengut, Neil Walker, et al.
Diabetes
|
April 29, 2006
No evidence for association of OAS1 with type 1 diabetes in unaffected siblings or type 1 diabetic cases
Deborah J Smyth, Jason D Cooper, Christopher E Lowe, et al.
American Journal of Human Genetics
|
June 24, 2003
Control of confounding of genetic associations in stratified populations
Clive J Hoggart, Eteban J Parra, Mark D Shriver, et al.
Page
of 17
Search research articles
Search
Showing results (111-120 of 169) with videos related to
Sort By:
Page
of 17
Biotechniques
|
May 22, 2004
SNP allele frequency estimation in DNA pools and variance components analysis
Kate Downes, Bryan J Barratt, Pelin Akan, et al.
Cardiovascular Research
|
July 1, 1989
Variable adaptation of molecular mechanisms in relation to the use of autologous striated muscle to augment myocardial function
C W Pattison, D V Cumming, D G Clayton Jones, et al.
Annals of the New York Academy of Sciences
|
January 1, 1985
Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia
S Pang, M S Pollack, M Loo, et al.
Journal of Vascular Surgery
|
December 18, 2001
Determinants of carotid microembolization
J Golledge, R Gibbs, C Irving, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 1, 1985
Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia
S Pang, M S Pollack, M Loo, et al.
The Journal of Pediatrics
|
April 17, 1998
Pulmonary function in hospitalized infants and toddlers with cystic fibrosis
R G Clayton, C E Diaz, N S Bashir, et al.
The Journal of Thoracic and Cardiovascular Surgery
|
November 1, 1991
Aortic counterpulsation for up to 28 days with autologous latissimus dorsi in sheep
C W Pattison, D V Cumming, A Williamson, et al.
Genetic Epidemiology
|
September 14, 2012
Validity of the family-based association test for copy number variant data in the case of non-linear intensity-genotype relationship
Manuela Zanda, Suna Onengut, Neil Walker, et al.
Diabetes
|
April 29, 2006
No evidence for association of OAS1 with type 1 diabetes in unaffected siblings or type 1 diabetic cases
Deborah J Smyth, Jason D Cooper, Christopher E Lowe, et al.
American Journal of Human Genetics
|
June 24, 2003
Control of confounding of genetic associations in stratified populations
Clive J Hoggart, Eteban J Parra, Mark D Shriver, et al.
Page
of 17