Human Genome Epidemiology Literature Finder
|
Records 1 - 3 (of 3 Records) |
| Query Trace: Asperger Syndrome and OXTR[original query] |
|---|
| Evidence for the involvement of genetic variation in the oxytocin receptor gene (OXTR) in the etiology of autistic disorders on high-functioning level. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010 Mar 153B (2): 629-39. Wermter Anne-Kathrin, Kamp-Becker Inge, Hesse Philipp, Schulte-Körne Gerd, Strauch Konstantin, Remschmidt Helm |
| Genetic variation in the oxytocin receptor (OXTR) gene is associated with Asperger Syndrome. Molecular autism 2014 5 (1): 48. Di Napoli Agnese, Warrier Varun, Baron-Cohen Simon, Chakrabarti Bhismad |
| Impaired social cognition processes in Asperger syndrome and anorexia nervosa. In search for endophenotypes of social cognition. Psychiatria polska 2016 50 (3): 533-42. Kasperek-Zimowska Beata Joanna, Zimowski Janusz Grzegorz, Biernacka Katarzyna, Kucharska-Pietura Katarzyna, Rybakowski Fil |
- Page last reviewed:Feb 1, 2024
- Content source:

