Showing results 1 to 6 of 6
Title | Author(s) | Issue Date | |
---|---|---|---|
2016 | |||
De novo C-terminal truncating mutations in MN1 cause a neurodevelopmental syndrome with distinctive facial features Proceeding/Conference:European Human Genetics Conference, 2019 | Gordon, CTLeung, KCMak, CCYDoherty, DLin, AVegas, NCho, MDimartino, CWeisfeld-Adams, JLessel, DJoss, SLi, CGonzaga-Jauregui, CZarate, YTroyer, CKant, SLeung, GBarone, AYang, SBend, ERoadhouse, CZahir, FStolerman, EBienvenu, TOrenstein, NDobyns, WShieh, JWaggoner, DGripp, KParker, MStoler, JLyonnet, SCormiere-Daire, VViskochil, DHoffman, TAmiel, JChung, BHY | 2019 | |
Excellent outcome of acute lymphoblastic leukaemia with TCF3-PBX1 rearrangement in Hong Kong Journal:Pediatric Blood & Cancer | 2018 | ||
Pathway analysis using random forests classification and regression Journal:Bioinformatics | 2006 | ||
Pharmacogenetic screening: HLA-B5701 vs. CYP2B6 G516T Journal:HIV Medicine | 2011 | ||
2011 |