Browsing by Author Waye, MMY

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TitleAuthor(s)Issue DateViews
 
2000
87
 
2000
243
 
Schizophrenia and hypocalcaemia: Variable phenotype of deletion at chromosome 22q11
Journal:Australian and New Zealand Journal of Psychiatry
1999
55
 
Frazer, KABallinger, DGCox, DRHinds, DAStuve, LLGibbs, RABelmont, JWBoudreau, AHardenbol, PLeal, SMPasternak, SWheeler, DAWillis, TDYu, FYang, HZeng, CGao, YHu, HHu, WLi, CLin, WLiu, SPan, HTang, XWang, JWang, WYu, JZhang, BZhang, QZhao, HZhao, HZhou, JGabriel, SBBarry, RBlumenstiel, BCamargo, ADefelice, MFaggart, MGoyette, MGupta, SMoore, JNguyen, HOnofrio, RCParkin, MRoy, JStahl, EWinchester, EZiaugra, LAltshuler, DShen, YYao, ZHuang, WChu, XHe, YJin, LLiu, YShen, YSun, WWang, HWang, YWang, YXiong, XXu, LWaye, MMYTsui, SKWXue, HWong, JTFGalver, LMFan, JBGunderson, KMurray, SSOliphant, ARChee, MSMontpetit, AChagnon, FFerretti, VLeboeuf, MOlivier, JFPhillips, MSRoumy, SSallée, CVerner, AHudson, TJKwok, PYCai, DKoboldt, DCMiller, RDPawlikowska, LTaillonMiller, PXiao, MTsui, LCMak, WYou, QSTam, PKHNakamura, YKawaguchi, TKitamoto, TMorizono, TNagashima, AOhnishi, YSekine, ATanaka, TTsunoda, TDeloukas, PBird, CPDelgado, MDermitzakis, ETGwilliam, RHunt, SMorrison, JPowell, DStranger, BEWhittaker, PBentley, DRDaly, MJDe Bakker, PIWBarrett, JChretien, YRMaller, JMcCarroll, SPatterson, NPe'Er, IPrice, APurcell, SRichter, DJSabeti, PSaxena, RSchaffner, SFSham, PCVarilly, PStein, LDKrishnan, LSmith, AVTelloRuiz, MKThorisson, GAChakravarti, AChen, PECutler, DJKashuk, CSLin, SAbecasis, GRGuan, WLi, YMunro, HMQin, ZSThomas, DJMcVean, GAuton, ABottolo, LCardin, NEyheramendy, SFreeman, CMarchini, JMyers, SSpencer, CStephens, MDonnelly, PCardon, LRClarke, GEvans, DMMorris, APWeir, BSJohnson, TAMullikin, JCSherry, STFeolo, MSkol, AZhang, HMatsuda, IFukushima, YMacEr, DRSuda, ERotimi, CNAdebamowo, CAAjayi, IAniagwu, TMarshall, PANkwodimmah, CRoyal, CDMLeppert, MFDixon, MPeiffer, AQiu, RKent, AKato, KNiikawa, NAdewole, IFKnoppers, BMFoster, MWClayton, EWWatkin, JMuzny, DNazareth, LSodergren, EWeinstock, GMYakub, IBirren, BWWilson, RKFulton, LLRogers, JBurton, JCarter, NPClee, CMGriffiths, MJones, MCMcLay, KPlumb, RWRoss, MTSims, SKWilley, DLChen, ZHan, HKang, LGodbout, MWallenburg, JCL'Archevêque, PBellemare, GSaeki, KWang, HAn, DFu, HLi, QWang, ZWang, RHolden, ALBrooks, LDMcEwen, JEGuyer, MSWang, VOPeterson, JLShi, MSpiegel, JSung, LMZacharia, LFCollins, FSKennedy, KJamieson, RStewart, J
2007
232
 
2005
39
 
Should we invest in BioBanking in Hong Kong?: Using BioBanking for dyslexic studies in Hong Kong as an example
Book:Human Genetic Biobanks in Asia: Politics of Trust and Scientifc Advancement
2008
82
 
2017
16
 
2004
165
 
2017
26
 
The relationship between delayed copying and spelling in Hong Kong children
Proceeding/Conference:Association for Reading and Writing in Asia Annual Conference
2017
19
 
The relationship between N1 print tuning and literacy in Chinese children
Proceeding/Conference:Annual Meeting of the Society for the Scientific Study of Reading, SSSR 2016
2016
26
 
2001
61
 
Velo-cardio-facial syndrome, schizophrenia at chromosome 22q11
Journal:Journal of Intellectual Disability Research
1998
35
 
2018
19