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Molecular Therapy : the Journal of the American Society of Gene Therapy|July 5, 2012
Valproic acid confers functional pluripotency to human amniotic fluid stem cells in a transgene-free approachDafni Moschidou, Sayandip Mukherjee, Michael P Blundell, et al.Genes|August 27, 2021
Wide Fontanels, Delayed Speech Development and Hoarse Voice as Useful Signs in the Diagnosis of KBG Syndrome: A Clinical Description of 23 Cases with Pathogenic Variants Involving the ANKRD11 Gene or Submicroscopic Chromosomal Rearrangements of 16q24.3Anna Kutkowska-Kaźmierczak, Maria Boczar, Ewa Kalka, et al.American Journal of Human Genetics|August 2, 2011
Characterization of a 8q21.11 microdeletion syndrome associated with intellectual disability and a recognizable phenotypeMaría Palomares, Alicia Delicado, Elena Mansilla, et al.European Journal of Human Genetics : EJHG|May 1, 2018
Comprehensive genomic analysis of patients with disorders of cerebral cortical developmentWojciech Wiszniewski, Pawel Gawlinski, Tomasz Gambin, et al.Nature Genetics|November 26, 2008
Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalitiesNicola Brunetti-Pierri, Jonathan S Berg, Fernando Scaglia, et al.American Journal of Obstetrics and Gynecology|September 17, 2023
Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of ageLindsay R Freud, Stephanie Galloway, T Blaine Crowley, et al.Pageof 6