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Clinical Genetics|March 1, 1994
Informativity of intragenic microsatellites for carrier detection and prenatal diagnosis of cystic fibrosis in the Italian populationC Magnani, L Cremonesi, E Belloni, et al.Mucosal Immunology|February 25, 2016
Group 3 innate lymphoid cells regulate neutrophil migration and function in human deciduaD Croxatto, A Micheletti, E Montaldo, et al.Neurology|December 17, 2008
Management and treatment of glycogenosis type IIB Bembi, E Cerini, C Danesino, et al.Human Mutation|January 1, 1992
Four new mutations of the CFTR gene (541delC, R347H, R352Q, E585X) detected by DGGE analysis in Italian CF patients, associated with different clinical phenotypesL Cremonesi, M Ferrari, E Belloni, et al.Human Mutation|January 1, 1995
Analysis of linkage disequilibrium between different cystic fibrosis mutations and three intragenic microsatellites in the Italian populationM P Russo, G Romeo, M Devoto, et al.Tumori|April 30, 1985
Lipid bound sialic acid in cancer patientsL Salvagno, E Ferrazzi, V C Sileni, et al.British Journal of Haematology|June 2, 2007
High serum levels of B-lymphocyte stimulator are associated with clinical-pathological features and outcome in classical Hodgkin lymphomaC Tecchio, G Nadali, P Scapini, et al.Gene|December 17, 2011
Carbamoyl phosphate synthetase 1 deficiency in Italy: clinical and genetic findings in a heterogeneous cohortS Funghini, J Thusberg, M Spada, et al.Journal of Immunology (Baltimore, Md. : 1950)|December 2, 1998
Involvement of the IP-10 chemokine in sarcoid granulomatous reactionsC Agostini, M Cassatella, R Zambello, et al.Pageof 11