HKU Scholars Hub: Browsing DSpace

Browsing by Author rp00453

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 中

or enter first few letters:

Showing results 115 to 134 of 181 < previous next >

Title	Author(s)	Issue Date
A new halo-pelvic apparatus Journal:Spine	Cheung, KMC Kwan, EYC Chan, KYK Luk, KDK	2003
A newborn with a 790 kb chromosome 17p13.3 microduplication presenting with aortic stenosis, microcephaly and dysmorphic facial features - Is cardiac assessment necessary for all patients with 17p13.3 microduplication? Journal:European Journal of Medical Genetics	Ho, ACC Liu, APY Lun, KS Tang, WF Chan, KYK Lau, EYT Tang, MHY Tan, TY Chung, BHY	2012
A novel subset of putative stem/progenitor CD34+Oct-4+ cells is the major target for SARS coronavirus in human lung Journal:Journal of Experimental Medicine	Chen, Y Chan, VSF Zheng, B Chan, KYK Xu, X To, LYF Huang, FP Khoo, US Lin, CLS	2007
Oct4 is Epigenetically Regulated by Methylation in Normal Placenta and Gestational Trophoblastic Disease Journal:Placenta	Zhang, HJ Siu, MKY Wong, ESY Wong, KY Li, ASM Chan, KYK Ngan, HYS Cheung, ANY	2008
Overexpression of NANOG in gestational trophoblastic diseases: Effect on apoptosis, cell invasion, and clinical outcome Journal:American Journal of Pathology	Siu, MKY Wong, ESY Hoi, YC Ngan, HYS Chan, KYK Cheung, ANY	2008
p73 Expression is associated with the cellular radiosensitivity in cervical cancer after radiotherapy Journal:Clinical Cancer Research	Liu, SS Leung, RCY Chan, KYK Chiu, PM Cheung, ANY Tam, KF Ng, TY Wong, LC Ngan, HYS	2004
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
Pathway analyses identify TGFBR2 as potential breast cancer susceptibility gene: results from a consortium study among Asians Journal:Cancer Epidemiology, Biomarkers & Prevention	Ma, X Beeghly-Fadiel, A Lu, W Shi, J Xiang, YB Cai, Q Shen, H Shen, CY Ren, Z Matsuo, K Khoo, US Iwasaki, M Long, J Zhang, B Ji, BT Zheng, Y Wang, W Hu, Z Liu, Y Wu, PE Shieh, YL Wang, S Xie, X Ito, H Kasuga, Y Chan, KYK Iwata, H Tsugane, S Gao, YT Shu, XO Moses, HL Zheng, W	2012
Polymorphisms of the ACE2 and CD13 (ANPEP) genes, and susceptibility to SARS coronavirus infection in Chinese from Hong Kong Proceeding/Conference:HUGO Annual Human Genome Meeting, HGM 2004	Chan, YK Song, Y Mak, WK Cheung, ANY Peiris, JSM Yip, SP Tin, PC Liu, W Xue, W Chan, LC Tam, PKH Ngan, HYS Khoo, US	2004
Polyomavirus enhancer activator 3 protein promotes breast cancer metastatic progression through Snail-induced epithelial-mesenchymal transition Journal:Journal of Pathology	Yuen, HF Chan, YK Grills, C McCrudden, CM Gunasekharan, V Shi, Z Wong, ASY Lappin, TR Chan, KW Fennell, DA Khoo, US Johnston, PG El-Tanani, M	2011
Population-based case-control study of HER2 genetic polymorphism in ovarian cancer Proceeding/Conference:Proceedings of the American Association for Cancer Research	Khoo, US Chan, YK Lai, TW Yip, SP Ko, HH Cheung, ANY	2002
Potentials and challenges of launching the pilot phase of Hong Kong Genome Project Journal:Journal of Translational Genetics and Genomics	Chu, ATW Fung, LF Tong, AHY Chow, SM Chan, YK Yeung, KS Lo, HM Chung, BHY	2022
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
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
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
Prenatal diagnosis and long‐term follow‐up of a Chinese patient with mosaic variegated aneuploidy and its molecular analysis Journal:Clinical Case Reports	LIN, SM LUK, HM LO, IFM TAM, WK Chan, KYK TSE, HY Leung, WC Tang, MHY Kan, ASY	2020
Prenatal diagnosis of 5p deletion syndrome: Report of five cases Journal:Journal of Obstetrics and Gynaecology Research	Mak, ASL Ma, TWL Chan, KYK Kan, ASY Tang, MHY Leung, KY	2019
Prenatal diagnosis of familial atretic encephalocele Journal:Ultrasound in Obstetrics and Gynecology	Lau, WL Yung, WY Leung, WC Kan, A Chan, K Luk, HM Kan, E Lam, YY	2019
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
Primary peritoneal malignant mixed mfcllerian tumors: A clinicopathologic, immunohistochemical, and genetic study Journal:Cancer	Shen, DH Khoo, US Xue, W Ngan, HYS Wang, JL Liu, VWS Chan, YK Cheung, ANY	2001

Showing results 115 to 134 of 181 < previous next >