Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression
暂无分享，去创建一个
S. Scherer | A. C. Lionel | C. Marshall | M. Tarnopolsky | R. Nicolson | A. Bassett | M. Nowaczyk | V. Siu | D. Stavropoulos | Chelsea Lowther | C. Prasad | M. Speevak | Chumei Li | P. Bikangaga | G. Graham | P. Dick | S. Zeesman | C. Armour | E. McCready | E. Goh | D. Samdup | Kerry Boyd | L. Schultz | A. Morra | Mostafa Zaazou | Jack H Jung | Manjulata Rajguru | S. Goobie | Asmaa S. Hussain | Margreet Walinga | Renske G Reijenga | Matthew J. Gazzellone | A. Hussain | Lee-Anne Schultz | Jack H. Jung