| Title : Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing - Jiang_2013_Am.J.Hum.Genet_93_249 |
| Author(s) :
Jiang YH , Yuen RK , Jin X , Wang M , Chen N , Wu X , Ju J , Mei J , Shi Y , He M , Wang G , Liang J , Wang Z , Cao D , Carter MT , Chrysler C , Drmic IE , Howe JL , Lau L , Marshall CR , Merico D , Nalpathamkalam T , Thiruvahindrapuram B , Thompson A , Uddin M , Walker S , Luo J , Anagnostou E , Zwaigenbaum L , Ring RH , Wang J , Lajonchere C , Shih A , Szatmari P , Yang H , Dawson G , Li Y , Scherer SW |
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Ref :
American Journal of Human Genetics , 93 :249 , 2013 |
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Abstract :
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| PubMedSearch : Jiang_2013_Am.J.Hum.Genet_93_249 |
| PubMedID: 23849776 |
| Gene_locus related to this paper:
human-NLGN3 |