Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: AUTS5[original query] |
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High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility. Molecular psychiatry 2010 Sep 15 (9): 954-68. Maestrini E, Pagnamenta A T, Lamb J A, Bacchelli E, Sykes N H, Sousa I, Toma C, Barnby G, Butler H, Winchester L, Scerri T S, Minopoli F, Reichert J, Cai G, Buxbaum J D, Korvatska O, Schellenberg G D, Dawson G, de Bildt A, Minderaa R B, Mulder E J, Morris A P, Bailey A J, Monaco A P, |
Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment. American journal of medical genetics. Part A 2009 Feb 149A (4): 588-97. Newbury Dianne F, Warburton Pamela C, Wilson Natalie, Bacchelli Elena, Carone Simona, , Lamb Janine A, Maestrini Elena, Volpi Emanuela V, Mohammed Shehla, Baird Gillian, Monaco Anthony |
Family-based association study of ZNF533, DOCK4 and IMMP2L gene polymorphisms linked to autism in a northeastern Chinese Han population. Journal of Zhejiang University. Science. B 2014 Mar 15 (3): 264-71. Liang Shuang, Wang Xue-lai, Zou Ming-yang, Wang Han, Zhou Xue, Sun Cai-hong, Xia Wei, Wu Li-jie, Fujisawa Takashi X, Tomoda Ake |
Identification of a homozygous missense mutation in LRP2 and a hemizygous missense mutation in TSPYL2 in a family with mild intellectual disability. Psychiatric genetics 2015 Nov . Vasli Nasim, Ahmed Iltaf, Mittal Kirti, Ohadi Mehrnaz, Mikhailov Anna, Rafiq Muhammad A, Bhatti Attya, Carter Melissa T, Andrade Danielle M, Ayub Muhammad, Vincent John B, John Pet |
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