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European Journal of Medical Genetics|August 16, 2017
Impairment of different protein domains causes variable clinical presentation within Pitt-Hopkins syndrome and suggests intragenic molecular syndromology of TCF4Maria Francesca Bedeschi, Giuseppe Marangi, Maria Rosaria Calvello, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 12, 2020
Huntingtin gene CAG repeat size affects autism risk: Family-based and case-control association studyIgnazio Stefano Piras, Chiara Picinelli, Raffaele Iennaco, et al.Plos One|July 7, 2011
Evidence of distinct tumour-propagating cell populations with different properties in primary human hepatocellular carcinomaFederico Colombo, Francesca Baldan, Silvia Mazzucchelli, et al.Cardiovascular Research|September 14, 2010
Human cardiac and bone marrow stromal cells exhibit distinctive properties related to their originAlessandra Rossini, Caterina Frati, Costanza Lagrasta, et al.Journal of Neurodevelopmental Disorders|May 27, 2026
Chromosome 22q13 terminal deletion size is associated with relevant clinical features in a sample of 63 Italian patients with Phelan-McDermid syndromeLaura Sandoni, Fethia Chehbani, Lisa Asta, et al.Molecular Genetics & Genomic Medicine|June 27, 2020
FARP-1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex familyFrancesca Cucinotta, Arianna Ricciardello, Laura Turriziani, et al.Pageof 3