Showing results (61-70 of 122) with videos related to
Sort By:
Pageof 13
Journal of the Neurological Sciences|July 30, 1999
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patientsM Gomez-Lira, C Perusi, M Mottes, et al.Human Genetics|October 1, 1995
A common beta hexosaminidase gene mutation in adult Sandhoff disease patientsM Gomez-Lira, A Sangalli, M Mottes, et al.Human Molecular Genetics|December 1, 1994
Severe (type III) osteogenesis imperfecta due to glycine substitutions in the central domain of the collagen triple helixA Forlino, F Zolezzi, M Valli, et al.Bone Marrow Transplantation|January 1, 1991
An assessment of chimeric transcript detection in CML patients after bone marrow transplantationG Martinelli, M Sessarego, P Gasparini, et al.Journal of Hypertension|June 8, 2001
Homozygosity for angiotensinogen 235T variant increases the risk of myocardial infarction in patients with multi-vessel coronary artery diseaseO Olivieri, C Stranieri, D Girelli, et al.Journal of Medical Genetics|August 27, 1998
Association of the FcepsilonRIbeta gene with bronchial hyper-responsiveness in an Italian populationE Trabetti, V Cusin, G Malerba, et al.Journal of Neuroimmunology|November 26, 2002
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosisM Gomez-Lira, G Moretto, D Bonamini, 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.Pageof 13