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Minerva Urologica E Nefrologica = the Italian Journal of Urology and Nephrology|February 12, 1998
[Insufficient correction of blood bicarbonate levels in biguanide lactic acidosis treated with CVVH and bicarbonate replacement fluids]F Mariano, F Goia, R Vincenti, et al.Biochemistry and Molecular Biology International|April 17, 1999
Cellular uptake and delivery monitoring of liposome/DNA complexes during in vitro transfection of CFTR geneA L Serafino, G Novelli, S Di Sario, et al.European Journal of Pediatrics|December 1, 1995
Noonan syndrome: structural abnormalities of the mitral valve causing subaortic obstructionB Marino, M G Gagliardi, M C Digilio, et al.Scandinavian Journal of Haematology|August 1, 1984
Cytogenetic findings in acute promyelocytic leukaemia. A report of 25 casesG Alimena, B Dallapiccola, M R De Cuia, et al.Human Genetics|January 1, 1991
Fragile sites and chromosome instability: the distribution of breaks induced by cis-diamine-dichloro-platinum (II) in Fanconi anemia lymphocyte culturesB Porfirio, D Smeets, L Beckers, et al.American Journal of Medical Genetics|April 1, 1990
Autosomal dominant polycystic kidney disease: a linkage evaluation of heterogeneity in Italy. Italian Collaborative Group on Polycystic Kidney DiseaseP Mandich, G Restagno, G Novelli, et al.Mutation Research|September 1, 1989
Identification of 4 ataxia telangiectasia cell lines hypersensitive to gamma-irradiation but not to hydrogen peroxideO Cantoni, P Sestili, M Fiorilli, et al.Neurogenetics|May 17, 2001
Dopamine D4 receptor (DRD4) polymorphism and adaptability trait during infancy: a longitudinal study in 1- to 5-month-old neonatesA De Luca, M Rizzardi, I Torrente, et al.Journal of Medical Genetics|April 5, 2003
Mapping of a new autosomal dominant non-syndromic hearing loss locus (DFNA43) to chromosome 2p12E Flex, M Mangino, M Mazzoli, et al.Journal of Medical Genetics|November 6, 2001
Coeliac disease in Williams syndromeA Giannotti, G Tiberio, M Castro, et al.Pageof 34