Showing results (81-90 of 102) with videos related to
Sort By:
Pageof 11
Scientific Reports|April 17, 2025
Human leukocyte antigen-G in hepatocellular carcinoma driven by chronic viral hepatitis or steatotic liver diseaseStefano Mocci, Andrea Perra, Roberto Littera, et al.Journal of Clinical Immunology|September 28, 2023
Antibody Deficiency in Patients with Biallelic KARS1 MutationsFrancesco Saettini, Fabiola Guerra, Grazia Fazio, et al.The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Monogenic Diabetes Accounts for 6.3% of Cases Referred to 15 Italian Pediatric Diabetes Centers During 2007 to 2012Maurizio Delvecchio, Enza Mozzillo, Giuseppina Salzano, et al.Human Mutation|November 10, 2018
Small supernumerary marker chromosomes: A legacy of trisomy rescue?Nehir Edibe Kurtas, Luciano Xumerle, Lorena Leonardelli, et al.European Journal of Human Genetics : EJHG|April 20, 2017
Haploinsufficiency for ANKRD11-flanking genes makes the difference between KBG and 16q24.3 microdeletion syndromes: 12 new casesFrancesca Novara, Berardo Rinaldi, Sanjay M Sisodiya, et al.Frontiers in Immunology|August 13, 2025
The role of HLA-G in primary biliary cholangitis and response to therapyMichela Miglianti, Stefano Mocci, Roberto Littera, et al.Frontiers in Immunology|June 21, 2023
A review of the main genetic factors influencing the course of COVID-19 in Sardinia: the role of human leukocyte antigen-GStefano Mocci, Roberto Littera, Luchino Chessa, et al.Journal of Medical Genetics|March 15, 2020
Customised next-generation sequencing multigene panel to screen a large cohort of individuals with chromatin-related disorderGabriella Maria Squeo, Bartolomeo Augello, Valentina Massa, et al.Human Genetics|December 18, 2020
Chiari 1 malformation and exome sequencing in 51 trios: the emerging role of rare missense variants in chromatin-remodeling genesAldesia Provenzano, Andrea La Barbera, Mirko Scagnet, et al.Human Mutation|December 30, 2014
Optimizing the molecular diagnosis of GALNS: novel methods to define and characterize Morquio-A syndrome-associated mutationsAnna Caciotti, Rodolfo Tonin, Miriam Rigoldi, et al.Pageof 11