Showing results (291-300 of 627) with videos related to

Sort By:
Pageof 63
European Journal of Human Genetics : EJHG|February 25, 2010
Paternal origin of the de novo constitutional t(11;22)(q23;q11)Tamae Ohye, Hidehito Inagaki, Hiroshi Kogo, et al.
American Journal of Medical Genetics. Part A|September 24, 2018
22q and two: 22q11.2 deletion syndrome and coexisting conditionsJennifer L Cohen, Terrence B Crowley, Daniel E McGinn, et al.
American Journal of Human Genetics|November 27, 2015
Histone Modifier Genes Alter Conotruncal Heart Phenotypes in 22q11.2 Deletion SyndromeTingwei Guo, Jonathan H Chung, Tao Wang, et al.
International Journal of Pediatric Otorhinolaryngology|September 5, 2020
Magnetic resonance angiography (MRA) in preoperative planning for patients with 22q11.2 deletion syndrome undergoing craniofacial and otorhinolaryngologic proceduresRotem Kimia, Lisa Elden, Julia Dailey, et al.
Pediatrics|May 3, 2008
Early diagnosis of fibrodysplasia ossificans progressivaFrederick S Kaplan, Meiqi Xu, David L Glaser, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 17, 2018
Musical auditory processing, cognition, and psychopathology in 22q11.2 deletion syndromeLucy Gao, Sunny X Tang, James J Yi, et al.
Platelets|December 15, 2023
A case-control study of bleeding risk in children with 22q11.2 deletion syndrome undergoing cardiac surgeryT Blaine Crowley, Ian Campbell, Abinaya Arulselvan, et al.
American Journal of Medical Genetics. Part A|December 31, 2003
Unexpected death and critical illness in Prader-Willi syndrome: report of ten individualsDavid A Stevenson, Theresa M Anaya, Jill Clayton-Smith, et al.
Pageof 63