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Bulletin De La Societe Internationale De Chirurgie
|
January 11, 1975
Computerized on-line analysis of pulmonary mechanics in patients undergoing cardiopulmonary bypass
K E Karlson, M Saklad, J Paliotta, et al.
Journal of Medical Genetics
|
February 5, 2008
Human Gene Mutation Database: towards a comprehensive central mutation database
P D Stenson, E Ball, K Howells, et al.
Psychosomatic Medicine
|
September 1, 1984
Plasma cortisol and beta-endorphin immunoreactivity in human obesity
M R Cohen, D Pickar, R M Cohen, et al.
Human Molecular Genetics
|
December 1, 1994
Disruption of a binding site for hepatocyte nuclear factor 1 in the protein C gene promoter is associated with hereditary thrombophilia
L P Berg, D A Scopes, A Alhaq, et al.
Annals of Neurology
|
January 26, 2012
Exome sequencing: dual role as a discovery and diagnostic tool
Chee-Seng Ku, David N Cooper, Constantin Polychronakos, et al.
Human Genetics
|
May 4, 2011
Delineating the Hemostaseome as an aid to individualize the analysis of the hereditary basis of thrombotic and bleeding disorders
Kim Fechtel, Marika L Osterbur, Hildegard Kehrer-Sawatzki, et al.
Genes
|
November 27, 2021
Chronic Pancreatitis: The True Pathogenic Culprit within the <i>SPINK1</i> N34S-Containing Haplotype Is No Longer at Large
Na Pu, Emmanuelle Masson, David N Cooper, et al.
Nucleic Acids Research
|
April 24, 2021
MutationTaster2021
Robin Steinhaus, Sebastian Proft, Markus Schuelke, et al.
Thrombosis Research
|
February 1, 1991
A single base-pair deletion in the protein C gene causing recurrent thromboembolism
C Grundy, H Plendl, W Grote, et al.
Pediatric Nephrology (Berlin, Germany)
|
June 26, 2020
Prediction of kidney failure in children with chronic kidney disease and obstructive uropathy
Yuri V Sebastião, Jennifer N Cooper, Brian Becknell, et al.
Page
of 144
Search research articles
Search
Showing results (601-610 of 1,439) with videos related to
Sort By:
Page
of 144
Bulletin De La Societe Internationale De Chirurgie
|
January 11, 1975
Computerized on-line analysis of pulmonary mechanics in patients undergoing cardiopulmonary bypass
K E Karlson, M Saklad, J Paliotta, et al.
Journal of Medical Genetics
|
February 5, 2008
Human Gene Mutation Database: towards a comprehensive central mutation database
P D Stenson, E Ball, K Howells, et al.
Psychosomatic Medicine
|
September 1, 1984
Plasma cortisol and beta-endorphin immunoreactivity in human obesity
M R Cohen, D Pickar, R M Cohen, et al.
Human Molecular Genetics
|
December 1, 1994
Disruption of a binding site for hepatocyte nuclear factor 1 in the protein C gene promoter is associated with hereditary thrombophilia
L P Berg, D A Scopes, A Alhaq, et al.
Annals of Neurology
|
January 26, 2012
Exome sequencing: dual role as a discovery and diagnostic tool
Chee-Seng Ku, David N Cooper, Constantin Polychronakos, et al.
Human Genetics
|
May 4, 2011
Delineating the Hemostaseome as an aid to individualize the analysis of the hereditary basis of thrombotic and bleeding disorders
Kim Fechtel, Marika L Osterbur, Hildegard Kehrer-Sawatzki, et al.
Genes
|
November 27, 2021
Chronic Pancreatitis: The True Pathogenic Culprit within the <i>SPINK1</i> N34S-Containing Haplotype Is No Longer at Large
Na Pu, Emmanuelle Masson, David N Cooper, et al.
Nucleic Acids Research
|
April 24, 2021
MutationTaster2021
Robin Steinhaus, Sebastian Proft, Markus Schuelke, et al.
Thrombosis Research
|
February 1, 1991
A single base-pair deletion in the protein C gene causing recurrent thromboembolism
C Grundy, H Plendl, W Grote, et al.
Pediatric Nephrology (Berlin, Germany)
|
June 26, 2020
Prediction of kidney failure in children with chronic kidney disease and obstructive uropathy
Yuri V Sebastião, Jennifer N Cooper, Brian Becknell, et al.
Page
of 144