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	Title	Author(s)	Issue Date
	Pulmonary vascular complications in children with chronic liver diseases Proceeding/Conference:HKPS / HKPNA 2006 Joint Annual Scientific Meeting	Chow, PCLun, KSChau, AKT	2006
	Current clinical status of long acting Factor IX-Fc (B-long). Proceeding/Conference:East Asia Hemophilia Forum (EAHF)	Chan, GCF	2011
	LRRC7 regulates neurite morphogenesis through mGluR5 Proceeding/Conference:Neuroscience 2016	Chong, CHNg, CPMak, HSLi, QMcAlonan, GMChan, SY	2016
	心功能的超聲學評價 Proceeding/Conference:第六屆中日小兒高峰論壇暨《小兒心臟電生理基礎及臨床應用進展》和《川崎病診斷與治療研究新進展》學習班	Cheung, YF	2015
	Cardiac dysfunction in childhood cancer survivors Proceeding/Conference:Annual Scientific Congress of the Hong Kong College of Cardiology, HKCC 2016	Cheung, YF	2016
	Cardiac Dysfunction in Childhood Cancer Survivors Proceeding/Conference:Oriental Congress of Pediatrics, OCP 2015	Cheung, YF	2015
	Application of NGS in paediatric patients in Hong Kong Proceeding/Conference:International Symposium in Kanagawa 2017: The Progress of Neonatal Medicine in Asia	Chung, BHY	2017
	Spinal Muscular Atrophy - Hong Kong experience Proceeding/Conference:Asian and Oceanian Myology Center Annual Scentific Meeting in conjunction with Taiwan Child Neurology Society Annual Meeting, 2016	Chan, HSS	2016
	Targeting neuoblastoma and its microenvironment with novel approach Proceeding/Conference:Asia-Pacific Symposium of Neuroblastoma, 2015	Chan, GCF	2015
	常見血液疾病及其治療最新進展 Proceeding/Conference:Changjiang Forum of Pediatric Development	Chan, GCF	2016
	Relapsed and refractory neuroblastoma Proceeding/Conference:Pediatric Oncology Symposium (第十届儿童肿瘤学术研讨会)	Chan, GCF	2015
	Computer-aided facial recognition of Chinese individuals with Angelman Syndrome in Hong Kong Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016	Mok, TKGFleischer, NLuk, HMChung, BHY	2016
	Use of chromosomal microarray in Hong Kong patients with autism spectrum disorder - implication of a copy number variation involving DPP10 Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2016	Chung, BHYMak, SLChiu, TALeung, KCMak, CCYChu, WYMok, TKGChan, YKKan, SYATang, MHYLau, ETKFung, CWLee, SL	2016
	Identification of a CFTR founder mutations, c.3068T>G:p.I1023R, which causes protein trafficking defects in Chinese patients with cystic fibrosis Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016	Leung, KCYing, DMak, CCYChen, XYXu, WYeung, KSChu, WYMok, TKGChau, SKCMcLuskey, JOng, WPTLeong, HYChan, YKYang, WChen, JHLi, AMLau, YLLee, SLChung, BHY	2016
	Use of clinical chromosomal microarray in Hong Kong Chinese patients with autism spectrum disorder - implication of a copy number variation involving DPP10 Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016	Chu, YWYLeung, KCMak, ASLChiu, TAMak, CCYMok, TKGTang, WFChan, YKTang, MHYLau, ETKSo, KWTao, QVFung, CWWong, VCNLee, SLMarshall, CScherer, SKan, SYAChung, BHY	2016
	Genetic diagnosis of early onset epilepsy by whole exome sequencing and chromosomal array in Hong Kong Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016	Tsang, HYLeung, KCMak, CCYChu, WYMu, XLee, SLChan, GCFYung, AWYChung, BHY	2016
	Mutations in ATP6V1E1 or ATP6V1A cause AR cutis laxia Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016	van Damme, TGardenchik, TMohamed, MGucerrero-Castillo, SFreisinger, PGuillemyn, BKariminejad, ADalloyaux, Dvan Kraaij, SLefeber, DJSyx, DSteyaert, WDe Rycke, RHotschen, AKamstccg, EJWong, SYvan Scherpenzeei, MJamali, PBrandt, UNijtmans, LKorenke, CChung, BHYMak, CCYHausser, IKornak, UFischer-Zirnsak, BStrom, TMMeitinger, TAlanay, YUtine, GELeung, PKCGhadcri-Soli, SCoucke, PSymoens, SDe Paepe, AThiel, CHaack, TBMalfair, FMorava, ECallewaert, B	2016
	Recurrent de novo missense mutations in PP1CB cause a novel rasopathy closely resembling Noonan syndrome with loose anagen hair (Reviewer choice) Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016	Gripp, KWAldinger, KABennett, JBaker, LTusi, JPowell-Hamilton, NStabley, DSol-Church, KTimms, ADobyns, WBde Man, ALarson, ASpruijt, LKoolen, DStevens, SJCStegmann, APANillesen, MWNorrhock, HVBelien, MNellist, MVerheijen, FWilems, PJChung, BHYDubbs, HBhoj, ESantani, AMcDougall, CZackai, EHRinne, TKWessels, MW	2016
	Identification of a novel homozygous missense mutation in ABR causing cerebellar hypoplasia with early lethality Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016	Leung, GKCYing, DShek, NWMChu, WYYeung, KSTang, MHYKan, SYAChan, YKIp, JKJYang, WLau, YLChung, BHY	2016
	Exome sequencing of a Chinese patient cohort with ID/ASD and macrocephaly/megalencephaly: Identification of a patient with biallelic PTEN mutations and others with germline/ post-zygotic mutations in PIK3C-AKT-mTOR pathway Proceeding/Conference:17th Manchester Dysmorphology Conference	Chung, BHYYeung, KSTso, WYWYing, DIp, JKJChu, WYLeung, KCMak, CCY	2016