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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1996
Detection of two different nonsense mutations in exon 44 of the PKD1 gene in two unrelated Italian families with severe autosomal dominant polycystic kidney diseaseA E Turco, S Rossetti, E Bresin, et al.
Clinical Genetics|November 1, 1995
A novel missense mutation in exon 3 of the COL4A5 gene associated with late-onset Alport syndromeA E Turco, S Rossetti, M O Biasi, et al.
Human Genetics|December 1, 1994
Complete detection of mutations in cystic fibrosis patients of Native American originB Mercier, O Raguénès, X Estivill, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|January 18, 2011
Upregulated expression of Toll-like receptor 4 in peripheral blood of ischaemic stroke patients correlates with cyclooxygenase 2 expressionS Ferronato, M G Lira, S Olivato, et al.
European Journal of Human Genetics : EJHG|December 7, 2000
Recommendations for quality improvement in genetic testing for cystic fibrosis. European Concerted Action on Cystic FibrosisE Dequeker, H Cuppens, J Dodge, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|September 1, 2001
Linkage to atopy on chromosome 19 in north-eastern Italian families with allergic asthmaS Venanzi, G Malerba, R Galavotti, et al.
Molecular and Cellular Probes|April 1, 1996
'Fingerprinting' of HLA-DQA by polymerase chain reaction and heteroduplex analysisG Martinelli, E Trabetti, P Farabegoli, et al.
ESMO Open|June 1, 2022
The European Medicines Agency review of sacituzumab govitecan for the treatment of triple-negative breast cancerS Michaleas, A Moreno Oliver, J Mueller-Berghaus, et al.
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