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Showing results 30 to 49 of 60 < previous next >

Title	Author(s)	Issue Date	Views
Genetic counseling/consultation in South-East Asia: A report from the workshop at the 10th Asia Pacific Conference on Human Genetics Journal:Journal of Genetic Counseling	Zayts, OA Sarangi, S Thong, MK Chung, BHY Lo, FM Kan, SYA Lee, MH Padilla, CD Cutiongco-de la Paz, EM Faradz, MHS Wasant, P	2013	80
Health professionals’ involvement and information provision in genetic counseling following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong Journal:International Journal of Gynecology & Obstetrics	So, PL Cheng, YKY Cheuk, KY Chiu, WK Mak, SL Mok, SL Lo, TK Yung, WK Lo, FMI Chung, BHY Kan, SYA Lee, CP Tang, MHY	2019	61
Homozygous Missense Mutation in ABR Causes Cerebellar Hypoplasia with Early Lethality - A New Condition Identified by Exome Sequencing? Proceeding/Conference:Hong Kong Journal of Paediatrics (New series)	Ying, D Shek, NWM Chu, WY Yeung, KS Leung, KC Tang, MHY Kan, SYA Chan, YK Chung, BHY	2014	67
Human placental exosomes induce maternal systemic immune tolerance by reprogramming circulating monocytes Journal:Journal of Nanobiotechnology	BAI, K Lee, CL Liu, X LI, J Cao, D Zhang, L Hu, D Li, H Hou, Y Xu, Y Kan, SYA Cheung, KW Ng, EHY Yeung, WSB Chiu, CN	2022	7
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, GKC Ying, D Shek, NWM Chu, WY Yeung, KS Tang, MHY Kan, SYA Chan, YK Ip, JKJ Yang, W Lau, YL Chung, BHY	2016	52
Identifying genetic mutations in patients with Rasopathies using a Next Generation Sequencing Diagnostic Pipeline in Hong Kong Proceeding/Conference:Hong Kong Journal of Paediatrics (New series)	Lo, IFM Leung, KC Luk, HM Tang, VHM Gao, W Wong, WL Tang, LYF Chu, WY Kan, SYA Tang, MHY Lam, STS Yang, W Ma, CH Jin, D Chan, YK Chung, BHY	2014	123
Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES) Journal:BMC Medical Genomics	Leung, KC Mak, CCY Fung, LF Wong, WHS Tsang, HY Yu, HC Pei, LCS Yeung, KS Mok, TKG Lee, CP Hui, PW Tang, MHY Chan, YK Liu, APY Yang, W Sham, PC Kan, SYA Chung, BHY	2018	111
Immunoprophylaxis Failure of Infants Born to Hepatitis B Carrier Mothers Following Routine Vaccination Journal:Clinical Gastroenterology and Hepatology	Cheung, KW Seto, TYM Kan, SYA Jalal, K Chee, WYY Wong, RMS Lee, CP Ng, EHY	2018
Implementation of Public Funded Genome Sequencing in Evaluation of Fetal Structural Anomalies Journal:Genes	So, PL Hui, AST Ma, TWL Shu, W Hui, PW Kong, CW Lo, TK Kan, ABC Kan, EYL Chong, SC Chung, BHY Luk, HM Choy, KW Kan, SYA Leung, WC	2022
Informed choice and decision making in women offered cell-free DNA prenatal genetic screening Journal:Prenatal Diagnosis	Lo, TK Chan, YK Kan, SYA So, PL Kong, CW Mak, SL Lee, CN	2017
Is congenital pulmonary airway malformation really a rare disease? Result of a prospective registry with universal antenatal screening program Journal:Pediatric Surgery International	Lau, CT Kan, SYA Shek, NWM Tam, PKH Wong, KKY	2017
Next Generation Sequencing in Prenatal Diagnosis Proceeding/Conference:12th Asia-Pacific Conference on Human Genetics "Genomic Medicine and Clinical Practice", Bangkok, Thailand, 8-10 November 2017	LEUNG, KC Kan, SYA Chung, BHY	2017	48
Next generation sequencing in prenatal diagnosis Proceeding/Conference:American Society of Human Genetics Annual Meeting, ASHG2017	Leung, GKC Mak, CCY Pei, SLC Tsang, MHY Yu, MHC Yeung, KS Mok, GTK Hui, APW Tang, MHY Chan, KYK Kan, SYA Chung, BHY	2017
Optimal timing of hepatitis B virus DNA quantification and clinical predictors for higher viral load during pregnancy Journal:Acta Obstetricia et Gynecologica Scandinavica	Cheung, KW Seto, MTY So, PL Wong, D Mak, SLA Lau, WL Wang, W Kan, SYA Lee, CP Ng, EHY	2019	54
Parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong Journal:Journal of Obstetrics and Gynaecology Research	So, PL Cheng, YKY Cheuk, KY Chiu, WK Mak, SL Mok, SL Lo, TK Yung, WK Lo, FM Chung, BHY Kan, SYA Lee, CP Tang, MHY	2017	109
Paternal uniparental disomy of chromosome 19 in a pair of monochorionic diamniotic twins with dysmorphic features and developmental delay Journal:Journal of Medical Genetics	Yeung, KS Ho, SP Lee, SL Kan, SYA Chan, YK Tang, MHY MAK, CCY Leung, KC So, PL Pfundt, R Marshall, CR Scherer, SW Choufani, S Weksberg, R Chung, BHY	2018	79
Pregnancy-associated plasma protein A for prediction of fetal growth restriction Journal:International Journal of Gynecology & Obstetrics	Lo, TK Chan, KY Chan, SCS Kan, SYA Hui, PW Tang, MHY	2015
A prenatal case of split-hand malformation associated with 17p13.3 triplication – A dilemma in genetic counseling Journal:European Journal of Medical Genetics	Luk, HM Wong, VCH Lo, IFM Chan, YK Lau, ETK Kan, SYA Tang, MHY Tang, WF She, WMK Chu, WY Sin, WK Chung, BHY	28-Jan-2014	88
Prenatal diagnosis and long term follow up of a patient with mosaic variegated aneuploidy and its molecular analysis Proceeding/Conference:22nd International Conference on Prenatal Diagnosis and Therapy, 2018	Lin, SM Luk, HM Kan, SYA Tam, WK Chan, KYK Tse, HY Leung, WC Tang, MHY	2018	35
Prenatal presentation in two fetuses with features of Beckwith Wiedemann syndrome—An unexpected diagnosis of androgenetic chimera and its clinical implications Journal:American Journal of Medical Genetics Part A	Yu, PT Shu, W Mok, SL Hui, PW Chan, LW Kwok, KY Chan, YK Lo, TK Chung, BHY Luk, HM Kan, SYA	2022	9

Showing results 30 to 49 of 60 < previous next >