Showing results (321-330 of 621) with videos related to

Sort By:
Pageof 63
Pathology Oncology Research : POR|January 27, 2012
Epigenetic and copy number variation analysis in retinoblastoma by MS-MLPAGabriella Livide, Maria Carmela Epistolato, Mariangela Amenduni, et al.
International Journal of Molecular Sciences|July 2, 2021
C9orf72 Intermediate Repeats Confer Genetic Risk for Severe COVID-19 Pneumonia Independently of AgeIsabella Zanella, Eliana Zacchi, Simone Piva, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
Intellectual disability, midface hypoplasia, facial hypotonia, and Alport syndrome are associated with a deletion in Xq22.3Jayson D Rodriguez, Shambhu S Bhat, Ilaria Meloni, et al.
European Journal of Medical Genetics|November 8, 2006
2q24-q31 deletion: report of a case and review of the literatureC Pescucci, R Caselli, S Grosso, et al.
American Journal of Medical Genetics. Part A|June 26, 2010
Syndromic mental retardation with thrombocytopenia due to 21q22.11q22.12 deletion: Report of three patientsEleni Katzaki, Gilles Morin, Marzia Pollazzon, et al.
Cancer Letters|February 23, 2008
Anti-angiogenetic effects of immune-reconstituted influenza virosomes assembled with parathyroid hormone-related protein derived peptide vaccinePierpaolo Correale, Maria Teresa Del Vecchio, Tommaso Renieri, et al.
American Journal of Medical Genetics. Part A|March 19, 2008
Delineation of the phenotype associated with 7q36.1q36.2 deletion: long QT syndrome, renal hypoplasia and mental retardationRossella Caselli, Maria Antonietta Mencarelli, Filomena Tiziana Papa, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
Creatine transporter defect diagnosed by proton NMR spectroscopy in males with intellectual disabilityMaria Antonietta Mencarelli, Maria Tassini, Marzia Pollazzon, et al.
World Neurosurgery|July 21, 2018
Use of Flow Diversion for the Treatment of Distal Circulation Aneurysms: A Multicohort StudyKrishnan Ravindran, Alejandro Enriquez-Marulanda, Peter T M Kan, et al.
Epilepsy & Behavior : E&B|August 24, 2010
Epilepsy in Rett syndrome: clinical and genetic featuresMaria Pintaudi, Maria Grazia Calevo, Aglaia Vignoli, et al.
Pageof 63