Human Genome Epidemiology Literature Finder
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Query Trace: CSDE1[original query] |
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Common genetic variants on 1p13.2 associate with risk of autism.
Molecular psychiatry 2014 Nov 19 (11): 1212-9. Xia K, Guo H, Hu Z, Xun G, Zuo L, Peng Y, Wang K, He Y, Xiong Z, Sun L, Pan Q, Long Z, Zou X, Li X, Li W, Xu X, Lu L, Liu Y, Hu Y, Tian D, Long L, Ou J, Liu Y, Li X, Zhang L, Pan Y, Chen J, Peng H, Liu Q, Luo X, Su W, Wu L, Liang D, Dai H, Yan X, Feng Y, Tang B, Li J, Miedzybrodzka Z, Xia J, Zhang Z, Luo X, Zhang X, St Clair D, Zhao J, Zhang |
Exome analysis of carotid body tumor. BMC medical genomics 2018 3 11 (Suppl 1): 17. Snezhkina Anastasiya V, Lukyanova Elena N, Kalinin Dmitry V, Pokrovsky Anatoly V, Dmitriev Alexey A, Koroban Nadezhda V, Pudova Elena A, Fedorova Maria S, Volchenko Nadezhda N, Stepanov Oleg A, Zhevelyuk Ekaterina A, Kharitonov Sergey L, Lipatova Anastasiya V, Abramov Ivan S, Golovyuk Alexander V, Yegorov Yegor E, Vishnyakova Khava S, Moskalev Alexey A, Krasnov George S, Melnikova Nataliya V, Shcherbo Dmitry S, Kiseleva Marina V, Kaprin Andrey D, Alekseev Boris Y, Zaretsky Andrew R, Kudryavtseva Anna |
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