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European Journal of Human Genetics : EJHG|January 22, 2004
Exclusion of an extracolonic disease modifier locus on chromosome 1p33-36 in a large Swiss familial adenomatous polyposis kindredM Plasilova, A M Russell, A Wanner, et al.The Journal of Experimental Medicine|May 1, 1974
A serum factor in chronic hypocomplementemic hephritis distinct from immunoglobulins and activating the alternate pathway of complementE H Vallota, O Götze, H L Spiegelberg, et al.Acta Haematologica|January 1, 1977
Loss of the Y chromosome from bone marrow cells of males with myeloproliferative disorders. Report of two cases and review of the literatureP E Dileo, H J Müller, H P Obrecht, et al.Blut|June 18, 1979
Pathological cell aggregates in bone marrow cultures from patients with various hematological diseasesC Nissen, B Elliott, P Groff, et al.The American Journal of Gastroenterology|September 25, 2001
Mutations of the cystic fibrosis gene in patients with chronic pancreatitisK Truninger, N Malik, R W Ammann, et al.Human Genetics|March 1, 1995
Sequence polymorphism in kringle IV 37 in linkage disequilibrium with the apolipoprotein (a) size polymorphismH G Kraft, C Haibach, A Lingenhel, et al.Cell Death and Differentiation|July 18, 2009
Survival, neuron-like differentiation and functionality of mesenchymal stem cells in neurotoxic environment: the critical role of erythropoietinL Danielyan, R Schäfer, A Schulz, et al.Journal of Cognitive Neuroscience|March 6, 2007
Selective visual dimension weighting deficit after left lateral frontopolar lesionsS Pollmann, K Mahn, B Reimann, et al.The EMBO Journal|October 1, 1992
Primary and secondary structure of the pore-forming peptide of pathogenic Entamoeba histolyticaM Leippe, E Tannich, R Nickel, et al.Diving and Hyperbaric Medicine|June 14, 2012
Diving Accident Guidelines of the German Society for Diving and Hyperbaric Medicine: Summary versionPeter H J Müller, Wilfried Beuster, Wolfgang Hühn, et al.Pageof 42