Search research articles
Contact Us
Filters
Showing results (261-270 of 1,438) with videos related to
Page
of 144
Sort By:
Science (New York, N.Y.)
|
July 3, 1987
A physiological basis for a theory of synapse modification
M F Bear, L N Cooper, F F Ebner
Human Genetics
|
February 1, 1990
Rapid detection of deletions in the Duchenne muscular dystrophy gene by PCR amplification of deletion-prone exon sequences
M Hentemann, J Reiss, M Wagner, et al.
Surgical Forum
|
January 1, 1973
Acute normovolemic anemia: effect on the adequacy and distribution of coronary blood flow
J Brazier, N Cooper, J V Maloney, et al.
Human Genetics
|
November 3, 1998
The molecular genetics of growth hormone deficiency
A M Procter, J A Phillips, D N Cooper
Eye (London, England)
|
January 1, 1987
Molecular genetic approaches to the analysis of human ophthalmic disease
D N Cooper, M Jay, S Bhattacharya, et al.
The Journal of Emergency Medicine
|
March 12, 2013
Odontogenic abscess
Michael N Cooper, Luis K Abrishamian, Kim I Newton
Journal of Medical Genetics
|
February 12, 2013
From the periphery to centre stage: de novo single nucleotide variants play a key role in human genetic disease
Chee-Seng Ku, Eng King Tan, David N Cooper
Expert Review of Molecular Diagnostics
|
May 24, 2012
The 'sequence everything' approach and personalized clinical decision challenges
Chee-Seng Ku, David N Cooper, Dimitrios H Roukos
Forensic Science, Medicine, and Pathology
|
April 15, 2015
Fatal hemorrhage from simple lacerations of the scalp
J R Hamilton, J P Sunter, P N Cooper
Optics Express
|
October 14, 2022
High-performance, additively-manufactured atomic spectroscopy apparatus for portable quantum technologies
S H Madkhaly, N Cooper, L Coles, et al.
Page
of 144
Search research articles
Search
Showing results (261-270 of 1,438) with videos related to
Sort By:
Page
of 144
Science (New York, N.Y.)
|
July 3, 1987
A physiological basis for a theory of synapse modification
M F Bear, L N Cooper, F F Ebner
Human Genetics
|
February 1, 1990
Rapid detection of deletions in the Duchenne muscular dystrophy gene by PCR amplification of deletion-prone exon sequences
M Hentemann, J Reiss, M Wagner, et al.
Surgical Forum
|
January 1, 1973
Acute normovolemic anemia: effect on the adequacy and distribution of coronary blood flow
J Brazier, N Cooper, J V Maloney, et al.
Human Genetics
|
November 3, 1998
The molecular genetics of growth hormone deficiency
A M Procter, J A Phillips, D N Cooper
Eye (London, England)
|
January 1, 1987
Molecular genetic approaches to the analysis of human ophthalmic disease
D N Cooper, M Jay, S Bhattacharya, et al.
The Journal of Emergency Medicine
|
March 12, 2013
Odontogenic abscess
Michael N Cooper, Luis K Abrishamian, Kim I Newton
Journal of Medical Genetics
|
February 12, 2013
From the periphery to centre stage: de novo single nucleotide variants play a key role in human genetic disease
Chee-Seng Ku, Eng King Tan, David N Cooper
Expert Review of Molecular Diagnostics
|
May 24, 2012
The 'sequence everything' approach and personalized clinical decision challenges
Chee-Seng Ku, David N Cooper, Dimitrios H Roukos
Forensic Science, Medicine, and Pathology
|
April 15, 2015
Fatal hemorrhage from simple lacerations of the scalp
J R Hamilton, J P Sunter, P N Cooper
Optics Express
|
October 14, 2022
High-performance, additively-manufactured atomic spectroscopy apparatus for portable quantum technologies
S H Madkhaly, N Cooper, L Coles, et al.
Page
of 144