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Orphanet Journal of Rare Diseases|January 25, 2025
Combined biochemical profiling and DNA sequencing in the expanded newborn screening for inherited metabolic diseases: the experience in an Italian reference centerSimona Fecarotta, Lorenzo Vaccaro, Alessandra Verde, et al.Nature Communications|May 17, 2023
Cellular population dynamics shape the route to human pluripotencyFrancesco Panariello, Onelia Gagliano, Camilla Luni, et al.Nature Communications|April 30, 2024
A case of T-cell acute lymphoblastic leukemia in retroviral gene therapy for ADA-SCIDDaniela Cesana, Maria Pia Cicalese, Andrea Calabria, et al.Biorxiv : the Preprint Server for Biology|January 23, 2024
Polygenic risk for schizophrenia converges on alternative polyadenylation as molecular mechanism underlying synaptic impairmentFlorian J Raabe, Anna Hausruckinger, Miriam Gagliardi, et al.Pageof 2