Contributions of common genetic variants to specific languages and to when a language is learned

por Wong, Patrick C. M., Kang, Xin, So, Hon-Cheong, Choy, Kwong Wai
Publicado 2022

Prevalence and heritability of handedness in a Hong Kong Chinese twin and singleton sample

por Zheng, Mo, McBride, Catherine, Ho, Connie Suk-Han, Chan, Jonathan Ka-Chun, Choy, Kwong Wai, Paracchini, Silvia
Publicado 2020

ASPM-lexical tone association in speakers of a tone language: Direct evidence for the genetic-biasing hypothesis of language evolution

por Wong, Patrick C. M., Kang, Xin, Wong, Kay H. Y., So, Hon-Cheong, Choy, Kwong Wai, Geng, Xiujuan
Publicado 2020

Diagnostic Yield of Exome Sequencing in Fetuses with Sonographic Features of Skeletal Dysplasias but Normal Karyotype or Chromosomal Microarray Analysis: A Systematic Review

por Tse, Kai Yeung, Surya, Ilham Utama, Irwinda, Rima, Leung, Kwok Yin, Ting, Yuen Ha, Cao, Ye, Choy, Kwong Wai
Publicado 2023

Transdifferentiation of periodontal ligament-derived stem cells into retinal ganglion-like cells and its microRNA signature

por Ng, Tsz Kin, Yung, Jasmine S. Y., Choy, Kwong Wai, Cao, Di, Leung, Christopher K. S., Cheung, Herman S., Pang, Chi Pui
Publicado 2015

Low-Pass Genome Sequencing-Based Detection of Paternity: Validation in Clinical Cytogenetics

por Li, Keying, Zhao, Yilin, Chau, Matthew Hoi Kin, Cao, Ye, Leung, Tak Yeung, Kwok, Yvonne K., Choy, Kwong Wai, Dong, Zirui
Publicado 2023

MicroRNA-183 suppresses cancer stem-like cell properties in EBV-associated nasopharyngeal carcinoma

por Cheung, Chartia Ching-Mei, Lun, Samantha Wei-Man, Chung, Grace Tin-Yun, Chow, Chit, Lo, Carman, Choy, Kwong-Wai, Lo, Kwok-Wai
Publicado 2016

Performance of chromosomal microarray for patients with intellectual disabilities/developmental delay, autism, and multiple congenital anomalies in a Chinese cohort

por Chong, Wilson Wai Sing, Lo, Ivan Fai Man, Lam, Stephen Tak Sum, Wang, Chi Chiu, Luk, Ho Ming, Leung, Tak Yeung, Choy, Kwong Wai
Publicado 2014

A γA-Crystallin Mouse Mutant Secc with Small Eye, Cataract and Closed Eyelid

por Cheng, Man Hei, Tam, Chung Nga, Choy, Kwong Wai, Tsang, Wai Hung, Tsang, Sze Lan, Pang, Chi Pui, Song, You Qiang, Sham, Mai Har
Publicado 2016

Sequencing data of cell-free DNA fragments in living-related liver transplantation for inborn errors of metabolism

por Zhu, Xiaofan, Ng, Hoi Ioi, Xuan, Liming, Long, Yan, Mao, Yan, Shi, Yu, Sun, Liying, Liang, Bo, Scaglia, Fernando, Zhu, Zhijun, Choy, Kwong Wai
Publicado 2020

First Case Report of Maternal Mosaic Tetrasomy 9p Incidentally Detected on Non-Invasive Prenatal Testing

por Shu, Wendy, Cheng, Shirley S. W., Xue, Shuwen, Chan, Lin Wai, Soong, Sung Inda, Kan, Anita Sik Yau, Cheung, Sunny Wai Hung, Choy, Kwong Wai
Publicado 2021

Immunopanning purification and long-term culture of human retinal ganglion cells

por Zhang, Xin-Mei, Li Liu, David Ta, Chiang, Sylvia Wai-Yee, Choy, Kwong-Wai, Pang, Chi-Pui, Lam, Dennis Shun-Chiu, Yam, Gary Hin-Fai
Publicado 2010

Prenatal diagnosis of complete maternal uniparental isodisomy of chromosome 4 in a fetus without congenital abnormality or inherited disease-associated variations

por Liu, WeiQiang, Zhang, HuiMin, Wang, Jian, Yu, GuoJiu, Qiu, WenJun, Li, ZhiHua, Chen, Min, Choy, Kwong Wai, Sun, XiaoFang
Publicado 2015

The Burden and Benefits of Knowledge: Ethical Considerations Surrounding Population-Based Newborn Genome Screening for Hearing

por Mitchell, Calli O., Rivera-Cruz, Greysha, Chau, Matthew Hoi Kin, Dong, Zirui, Choy, Kwong Wai, Shen, Jun, Amr, Sami, Giersch, Anne B. S., Morton, Cynthia C.
Publicado 2022

Local administration of siRNA through Microneedle: Optimization, Bio-distribution, Tumor Suppression and Toxicity

por Tang, Tao, Deng, Yan, Chen, Jiao, Zhao, Yi, Yue, Ruifeng, Choy, Kwong Wai, Wang, Chi Chiu, Du, Quan, Xu, Yan, Han, Linxiao, Chung, Tony Kwok Hung
Publicado 2016

Trio-Based Low-Pass Genome Sequencing Reveals Characteristics and Significance of Rare Copy Number Variants in Prenatal Diagnosis

por Chau, Matthew Hoi Kin, Qian, Jicheng, Chen, Zihan, Li, Ying, Zheng, Yu, Tse, Wing Ting, Kwok, Yvonne K., Leung, Tak Yeung, Dong, Zirui, Choy, Kwong Wai
Publicado 2021

Investigation of the genetic etiology in male infertility with apparently balanced chromosomal structural rearrangements by genome sequencing

por Chau, Matthew Hoi Kin, Li, Ying, Dai, Peng, Shi, Mengmeng, Zhu, Xiaofan, Wah Chung, Jacqueline Pui, Kwok, Yvonne K, Choy, Kwong Wai, Kong, Xiangdong, Dong, Zirui
Publicado 2022

Resolving the genetic heterogeneity of prelingual hearing loss within one family: Performance comparison and application of two targeted next generation sequencing approaches

por Lu, Yu, Zhou, Xueya, Jin, Zhanguo, Cheng, Jing, Shen, Weidong, Ji, Fei, Liu, Liyang, Zhang, Xuegong, Zhang, Michael, Cao, Ye, Han, Dongyi, Choy, KwongWai, Yuan, Huijun
Publicado 2014

Clinical Implementation of Expanded Carrier Screening in Pregnant Women at Early Gestational Weeks: A Chinese Cohort Study

por Shi, Mengmeng, Liauw, Angeline Linna, Tong, Steve, Zheng, Yu, Leung, Tak Yeung, Chong, Shuk Ching, Cao, Ye, Lau, Tze Kin, Choy, Kwong Wai, Chung, Jacqueline P. W.
Publicado 2021

Low-pass genome sequencing-based detection of absence of heterozygosity: validation in clinical cytogenetics

por Dong, Zirui, Chau, Matthew Hoi Kin, Zhang, Yanyan, Yang, Zhenjun, Shi, Mengmeng, Wah, Yi Man, Kwok, Yvonne K., Leung, Tak Yeung, Morton, Cynthia C., Choy, Kwong Wai
Publicado 2021