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Human Genetics|February 19, 2017
Emerging genotype-phenotype relationships in patients with large NF1 deletionsHildegard Kehrer-Sawatzki, Victor-Felix Mautner, David N CooperGenetic Testing|September 4, 2004
Certificates of confidentiality in research: rationale and usageZachary N Cooper, Robert M Nelson, Lainie Friedman RossThe Journal of Biological Chemistry|July 25, 1983
Discoidin-binding polysaccharide from Dictyostelium discoideumD N Cooper, S C Lee, S H BarondesNucleic Acids Research|February 11, 1983
Unmethylated domains in vertebrate DNAD N Cooper, M H Taggart, A P BirdScience (New York, N.Y.)|July 3, 1987
A physiological basis for a theory of synapse modificationM F Bear, L N Cooper, F F EbnerHuman Genetics|February 1, 1990
Rapid detection of deletions in the Duchenne muscular dystrophy gene by PCR amplification of deletion-prone exon sequencesM Hentemann, J Reiss, M Wagner, et al.Human Genetics|November 3, 1998
The molecular genetics of growth hormone deficiencyA M Procter, J A Phillips, D N CooperEye (London, England)|January 1, 1987
Molecular genetic approaches to the analysis of human ophthalmic diseaseD N Cooper, M Jay, S Bhattacharya, et al.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 diseaseChee-Seng Ku, Eng King Tan, David N CooperForensic Science, Medicine, and Pathology|April 15, 2015
Fatal hemorrhage from simple lacerations of the scalpJ R Hamilton, J P Sunter, P N CooperPageof 123