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American Journal of Medical Genetics. Part A|September 27, 2014
Recurrent ∼100 Kb microdeletion in the chromosomal region 14q11.2, involving CHD8 gene, is associated with autism and macrocephalyPaolo Prontera, Valentina Ottaviani, Daniela Toccaceli, et al.International Journal of Molecular Sciences|September 21, 2017
Juvenile Moyamoya and Craniosynostosis in a Child with Deletion 1p32p31: Expanding the Clinical Spectrum of 1p32p31 Deletion Syndrome and a Review of the LiteraturePaolo Prontera, Daniela Rogaia, Amedea Mencarelli, et al.American Journal of Medical Genetics. Part A|June 18, 2016
A novel MED12 mutation: Evidence for a fourth phenotypePaolo Prontera, Valentina Ottaviani, Daniela Rogaia, et al.Neurogenetics|August 18, 2014
DPP6 gene disruption in a family with Gilles de la Tourette syndromePaolo Prontera, Valerio Napolioni, Valentina Ottaviani, et al.Blood|May 29, 2015
2p15-p16.1 microdeletions encompassing and proximal to BCL11A are associated with elevated HbF in addition to neurologic impairmentAlister P W Funnell, Paolo Prontera, Valentina Ottaviani, et al.Nature Immunology|July 21, 2026
Dysbiosis-induced expansion of AXL-positive inflammatory type 3 dendritic cells triggers preclinical autoimmunityGrozdan Cvijetic, Valentina Ottaviani, Isabella O Conway, et al.Pageof 1