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11. No evidence for involvement of genetic variants in the X-linked neuroligin genes NLGN3 and NLGN4X in probands with autism spectrum disorder on high functioning level. Wermter AK, Kamp-Becker I, Strauch K, Schulte-Körne G, Remschmidt H. Am J Med Genet B Neuropsychiatr Genet; 2008 Jun 05; 147B(4):535-7. PubMed ID: 18189281 [Abstract] [Full Text] [Related]
13. X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family. Laumonnier F, Bonnet-Brilhault F, Gomot M, Blanc R, David A, Moizard MP, Raynaud M, Ronce N, Lemonnier E, Calvas P, Laudier B, Chelly J, Fryns JP, Ropers HH, Hamel BC, Andres C, Barthélémy C, Moraine C, Briault S. Am J Hum Genet; 2004 Mar 05; 74(3):552-7. PubMed ID: 14963808 [Abstract] [Full Text] [Related]
14. A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort. Yu J, He X, Yao D, Li Z, Li H, Zhao Z. Behav Brain Funct; 2011 May 14; 7():13. PubMed ID: 21569590 [Abstract] [Full Text] [Related]
17. Analysis of the neuroligin 4Y gene in patients with autism. Yan J, Feng J, Schroer R, Li W, Skinner C, Schwartz CE, Cook EH, Sommer SS. Psychiatr Genet; 2008 Aug 14; 18(4):204-7. PubMed ID: 18628683 [Abstract] [Full Text] [Related]
18. Variations analysis of NLGN3 and NLGN4X gene in Chinese autism patients. Xu X, Xiong Z, Zhang L, Liu Y, Lu L, Peng Y, Guo H, Zhao J, Xia K, Hu Z. Mol Biol Rep; 2014 Jun 14; 41(6):4133-40. PubMed ID: 24570023 [Abstract] [Full Text] [Related]