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Genes|October 23, 2021
Atypical NF1 Microdeletions: Challenges and Opportunities for Genotype/Phenotype Correlations in Patients with Large NF1 DeletionsHildegard Kehrer-Sawatzki, Ute Wahlländer, David N Cooper, et al.Human Genetics|December 1, 1994
Determinants of the factor IX mutational spectrum in haemophilia B: an analysis of missense mutations using a multi-domain molecular model of the activated proteinA I Wacey, M Krawczak, V V Kakkar, et al.Academic Pediatrics|November 18, 2020
Differences in Tonsillectomy Utilization by Race/Ethnicity, Type of Health Insurance, and RuralityJennifer N Cooper, Swapna Koppera, Emily F Boss, et al.Plos One|July 11, 2015
Mutations Causing Complex Disease May under Certain Circumstances Be Protective in an Epidemiological SenseSabine Siegert, Andreas Wolf, David N Cooper, et al.International Archives of Allergy and Applied Immunology|January 1, 1987
Antibody synthesis in the rat liver: an association between antibody-forming cells in the liver and biliary antibodies following intravenous injection of horse erythrocytesL Carter, P J Barrington, G N Cooper, et al.Human Genetics|January 7, 1998
Homology modelling of the catalytic domain of early mammalian protein C: evolution of structural featuresA I Wacey, M Krawczak, G Kemball-Cook, et al.Human Genetics|January 1, 1992
Single-strand conformation polymorphism (SSCP) analysis of exon 11 of the CFTR gene reliably detects more than one third of non-delta F508 mutations in German cystic fibrosis patientsJ Plieth, F Rininsland, M Schlösser, et al.Journal of Strength and Conditioning Research|October 2, 2018
Effects of Lower-Body Muscular Fatigue on Vertical Jump and Balance PerformanceChristina N Cooper, Nicole C Dabbs, Judith Davis, et al.International Journal of Oncology|January 26, 1999
Differential expression of endogenous galectin-1 and galectin-3 in human prostate cancer cell lines and effects of overexpressing galectin-1 on cell phenotypeJ Ellerhorst, T Nguyen, D N Cooper, et al.Human Genetics|August 1, 1992
A novel homozygous missense mutation in the protein C (PROC) gene causing recurrent venous thrombosisC B Grundy, M Chisholm, V V Kakkar, et al.Pageof 123