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Showing results 8 to 15 of 15 < previous

	Title	Author(s)	Issue Date
	Increasing prenatal diagnosis of chimeras with the use of noninvasive prenatal screening: Report of two cases Journal:Prenatal Diagnosis	Yu, FNY Li, EYY Kong, MCW Ma, TWL Chan, KYK Man, E Chung, BHY Kan, ASY	2021
	Massive parallel sequencing for the genetic diagnosis of rasopathies: a study of 58 Chinese patients in Hong Kong Proceeding/Conference:Annual Scientific Meeting of the Canadian College of Medical Geneticists, CCMG 2013	Lo, IFM Leung, KC Luk, MHM Wong, WL Tang, LYF Chu, YWY Kan, ASY Tang, MHY Lam, STS Yang, W Chan, YK Chung, BHY	2013
	Prenatal and postnatal diagnosis of Schuurs‐Hoeijmakers syndrome: Case series and review of the literature Journal:American Journal of Medical Genetics Part A	Seto, MTY Bertoli-Avella, AM Cheung, KW Chan, KYK Yeung, KS Fung, JLF Beetz, C Bauer, P Luk, HM Lo, IFM Lee, CP Chung, BHY Kan, ASY	2021
	Prenatal diagnosis of Myhre syndrome with a heterozygous pathogenic variant in <i>SMAD4</i> gene presented with thick nuchal translucency and cardiac abnormalities Journal:Prenatal Diagnosis	Hui, PW Mok, YK Luk, HM Au, SLK Lau, EYT Chung, B Kan, ASY	2-Aug-2023
	Spread of X Inactivation on Chromosome 15 is Associated with a More Severe Phenotype in a Girl with an Unbalanced t(X;15) Translocation Journal:American Journal of Medical Genetics Part A	Yeung, KS Chee, WYY Luk, HM Kan, ASY Tang, MHY Lau, ETK Shuen, AY Lo, IFM Chan, YK Chung, BHY	2014
	The KLHL40 c.1516A>C is a Chinese‐specific founder mutation causing nemaline myopathy 8: Report of six patients with pre‐ and postnatal phenotypes Journal:Molecular Genetics & Genomic Medicine	Yeung, KS Yu, FNY Fung, CW Wong, S Lee, HCH Fung, STH Fung, GPG Leung, KY Chung, WH Lee, YT Ng, VKS YU, HC Fung, JLF TSANG, MHY Chan, KYK Chan, SHS Kan, ASY Chung, BHY	2020
	Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving DPP10 Journal:Molecular Autism	Mak, ASL Chiu, TA Leung, KC Mak, CCY Chu, WY Mok, TKG Tang, WF Chan, YK Tang, MHY Lau, ETK So, KW Tao, QV Fung, CW Wong, CNV Uddin, M Lee, SL Marshall, CR Scherer, SW Kan, ASY Chung, BHY	2017
	An X-linked dominant mutation in LAMP2 causing Danon disease associated with myotonia expanding the spectrum Proceeding/Conference:Neuromuscular Disorders	Chan, SHS Kan, ASY Tse, HF	2013

Showing results 8 to 15 of 15 < previous