A Genomewide Screen for Autism: Strong Evidence for Linkage to Chromosomes 2q, 7q, and 16p
*·2001·The American Journal of Human Genetics
DOI 10.1086/323264
Cited by (453)
Items 101–200 of 453
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- Mutation screening and association analysis of six candidate genes for autism on chromosome 7qElena Bonora, Janine A. Lamb, Gabrielle Barnby, Nuala Sykes, Thomas Moberly, Kim S. Beyer, Sabine M. Klauck, F. Poustka, Elena Bacchelli, Francesca Blasi et al. · 2004 · European Journal of Human Genetics
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- Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autismAnne Philippi, Elke Roschmann, Frédéric Torès, Pierre Lindenbaum, Abdel Benajou, L Germain-Leclerc, Charles Marcaillou, Karine Fontaine, Maud Vanpeene, Sudipta Singha Roy et al. · 2005 · Molecular Psychiatry
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- Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohortGuo, Hui, Peng, Yu, Hu, Zhengmao, Li, Ying, Xun, Guanglei, Ou, Jianjun, Sun, Liangdan, Xiong, Zhimin, Liu, Yanling, Wang, Tianyun et al. · 2017 · Scientific Reports
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