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European Journal of Human Genetics : EJHG|September 12, 2000
Increased frequency of CFTR gene mutations in sarcoidosis: a case/control association studyC Bombieri, M Luisetti, F Belpinati, et al.Journal of Medical Genetics|May 5, 1999
Association of a lymphotoxin alpha gene polymorphism and atopy in Italian familiesE Trabetti, C Patuzzo, G Malerba, et al.Cancer Genetics and Cytogenetics|May 1, 1993
Molecular analysis of six variant Philadelphia chromosome translocations in chronic myeloid leukemiaM Sessarego, G Martinelli, A Chiamenti, et al.Journal of Medical Genetics|December 1, 1994
Determination of a new collagen type I alpha 2 gene point mutation which causes a Gly640 Cys substitution in osteogenesis imperfecta and prenatal diagnosis by DNA hybridisationM Gomez-Lira, A Sangalli, P F Pignatti, et al.European Journal of Biochemistry|February 1, 1993
Osteogenesis imperfecta and type-I collagen mutations. A lethal variant caused by a Gly910-->Ala substitution in the alpha 1 (I) chainM Valli, A Sangalli, A Rossi, et al.ESMO Open|January 10, 2021
The EMA assessment of encorafenib in combination with cetuximab for the treatment of adult patients with metastatic colorectal carcinoma harbouring the BRAFV600E mutation who have received prior therapyA Trullas, J Delgado, J Koenig, et al.European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|December 4, 2003
No linkage or association of five polymorphisms in the interleukin-4 receptor alpha gene with atopic asthma in Italian familiesC Migliaccio, C Patuzzo, G Malerba, et al.Human Genetics|July 1, 1992
Mild dominant osteogenesis imperfecta with intrafamilial variability: the cause is a serine for glycine alpha 1(I) 901 substitution in a type-I collagen geneM Mottes, A Sangalli, M Valli, et al.European Journal of Cancer (Oxford, England : 1990)|September 1, 1995
Intrapatient comparison of single-agent epirubicin with or without lonidamine in metastatic breast cancerM Lopez, P Vici, L Di Lauro, et al.Human Mutation|January 1, 1993
Screening of 62 mutations in a cohort of cystic fibrosis patients from north eastern Italy: their incidence and clinical features of defined genotypesP Gasparini, C Marigo, G Bisceglia, et al.Pageof 15