HuGE Literature Finder
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Mutation screening in the Greek population and evaluation of NLGN3 and NLGN4X genes causal factors for autism. Psychiatric genetics 2013 Oct 23 (5): 198-203. Volaki Konstantina, Pampanos Andreas, Kitsiou-Tzeli Sophia, Vrettou Christina, Oikonomakis Vasilis, Sofocleous Christalena, Kanavakis Emmanu |
Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders. European journal of human genetics : EJHG 2013 Mar 21 (3): 310-6. Boccuto Luigi, Lauri Maria, Sarasua Sara M, Skinner Cindy D, Buccella Daniela, Dwivedi Alka, Orteschi Daniela, Collins Julianne S, Zollino Marcella, Visconti Paola, Dupont Barb, Tiziano Danilo, Schroer Richard J, Neri Giovanni, Stevenson Roger E, Gurrieri Fiorella, Schwartz Charles |
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- Page last updated:Mar 22, 2023
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