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Showing results 6 to 20 of 20 < previous

	Title	Author(s)	Issue Date	Views
	Identification of 21 novel and 3 known FBN1 mutations in 66 unrelated Chinese probands with Marfan syndrome or Marfan-like phenotypes Proceeding/Conference:Annual Congress of the Asian Society for Pediatric Research, ASPR 2006	Chung, BHY Lam, STS Tong, TMF Li, YH Lun, KS Chan, HC Or, SF Lau, YL	2006	114
	Identification of 21 novel and 3 known FBN1 mutations in 66 unrelated Chinese probands with Marfan syndrome or Marfan-like phenotypes Proceeding/Conference:HUGO / HUGO-AP 2006	Lun, KS Lam, STS Tong, TMF Chung, BHY Li, YH Chan, HC Or, SF Lau, YL	2006	101
	Identification of 22q11.2 deletion in patients from adult congenital heart disease clinic - a missed burden in the transition care Proceeding/Conference:European Journal of Human Genetics	Chung, B Chow, P Liu, A Lee, P Wong, V Chan, K Tang, M Lun, KS Lau, ETK Cheung, YF Chau, KT Lau, YL	2013	69
	Identification of 25 novel and 2 known FBN1 mutations in 66 unrelated Chinese probands with Marfan syndrome or Marfan-like phenotypes Proceeding/Conference:HKPS-HKPNA 2006 Joint Annual Scientific Meeting	Chung, BHY Lam, STS Tong, TMF Li, YH Lun, KS Chan, HC Or, SF Lau, YL	2006
	Identification of 7 novel TGFBR2 (Transforming Growth Factor-Beta Receptor 2) mutations in Chinese with Marfan syndrome (MFS) and related phenotypes using denaturing high performance liquid chromatography (DHPLC) Proceeding/Conference:International Congress of Pediatrics, IPA 2007	Chung, BHY Li, YH Lam, STS Yang, W Lun, KS Lau, YL	2007
	Identification of 7 novel TGFBR2 mutations in Chinese with marfan syndrome (MFS) and related phenotypes using DHPLC Proceeding/Conference:Congress of Asian Society for Pediatric Research, ASPR 2007	Chung, BHY Li, YH Lam, STS Yang, W Lun, KS Lau, YL	2007	106
	Identification of 7 novel transforming growth factor β receptor 2 mutations in Chinese patients with marfan syndrome Proceeding/Conference:Pediatrics	Chung, BHY Li, YH Lam, STS Yang, W Lun, KS Lau, YL	2008
	Identification of TAZ mutation in a family with X-linked dilated cardiomyopathy by Next Generation Sequencing Proceeding/Conference:European Journal of Human Genetics	Chung, B Man, E Yung, TC Lun, KS Chau, AKT	2012	173
	Impact of temporary interruption of long-term right ventricular pacing on left ventricular function and dyssynchrony in children and young adults congenital and acquired heart block Proceeding/Conference:World Congress of Paediatric Cardiology & Cardiac Surgery, WCPCCS 2009	Hong, W Yung, TC Lun, KS Cheung, YF	2009	113
	Impact of temporary interruption of long-term right ventricular pacing on left ventricular function and dyssynchrony in children and young adults with congenital and acquired heart block Proceeding/Conference:Congress of Asian Society for Pediatric Research, ASPR 2009	Hong, WJ Weng, DH Lun, KS Cheung, YF	2009	104
	Outcome of pregnancy in women with congential heart diseases (CHD) of a tertiary centre in Hong Kong Proceeding/Conference:Annual Scientific Congress of the Hong Kong College of Cardiology, HKCC 2013	Chow, PC Chan, KW Lun, KS Yung, TC Cheung, YF Chau, AKT	2013	34
	Outcome of thoracic organ transplantation for adults with congenital heart disease Proceeding/Conference:Journal of the Hong Kong College of Cardiology	Lun, KS Fan, K Wong, CF Yung, TC Chow, PC Wong, KT Cheung, YF Chow, WH Chau, AKT Chiu, SW Cheng, LC	2010
	Posterior Reversible Encephalopathy Syndrome: paediatric heart transplant with cyclosporine neurotoxicity Proceeding/Conference:Hong Kong Medical Journal	Tso, WWY Yung, AWY Lun, KS Yung, TC Fan, K Wong, VCN	2009	113
	Pulmonary vascular complications in children with chronic liver diseases Proceeding/Conference:HKPS / HKPNA 2006 Joint Annual Scientific Meeting	Chow, PC Lun, KS Chau, AKT	2006	30
	Two Chinese patients with Loeys-Dietz Syndrome due to TGFBR2 mutations Proceeding/Conference:Hong Kong Journal of Paediatrics (New series)	Chung, BHY Chan, SY Chow, PC Wong, KT Lun, KS Chau, KT Lau, YL	2011	154

Showing results 6 to 20 of 20 < previous