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

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

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

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

TEDD: a database of temporal gene expression patterns during multiple developmental periods in human and model organisms

por Zhou, Ziheng, Tan, Cong, Chau, Matthew Hoi Kin, Jiang, Xiaosen, Ke, Ziyuan, Chen, Xiaoyan, Cao, Ye, Kwok, Yvonne K, Bellgard, Matthew, Leung, Tak Yeung, Choy, Kwong Wai, Dong, Zirui
Publicado 2022

Clinical Significance of Non-Invasive Prenatal Screening for Trisomy 7: Cohort Study and Literature Review

por Zhu, Xiaofan, Lam, Doris Yuk Man, Chau, Matthew Hoi Kin, Xue, Shuwen, Dai, Peng, Zhao, Ganye, Cao, Ye, Cheung, Sunny Wai Hung, Kwok, Yvonne Ka Yin, Choy, Kwong Wai, Kong, Xiangdong, Leung, Tak Yeung
Publicado 2020

Investigation of Chromosomal Structural Abnormalities in Patients With Undiagnosed Neurodevelopmental Disorders

por Cao, Ye, Luk, Ho Ming, Zhang, Yanyan, Chau, Matthew Hoi Kin, Xue, Shuwen, Cheng, Shirley S. W., Li, Albert Martin, Chong, Josephine S. C., Leung, Tak Yeung, Dong, Zirui, Choy, Kwong Wai, Lo, Ivan Fai Man
Publicado 2022

Prenatal Diagnosis of Fetuses With Increased Nuchal Translucency by Genome Sequencing Analysis

por Choy, Kwong Wai, Wang, Huilin, Shi, Mengmeng, Chen, Jingsi, Yang, Zhenjun, Zhang, Rui, Yan, Huanchen, Wang, Yanfang, Chen, Shaoyun, Chau, Matthew Hoi Kin, Cao, Ye, Chan, Olivia Y.M., Kwok, Yvonne K., Zhu, Yuanfang, Chen, Min, Leung, Tak Yeung, Dong, Zirui
Publicado 2019

Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis

por Wang, Huilin, Dong, Zirui, Zhang, Rui, Chau, Matthew Hoi Kin, Yang, Zhenjun, Tsang, Kathy Yin Ching, Wong, Hoi Kin, Gui, Baoheng, Meng, Zhuo, Xiao, Kelin, Zhu, Xiaofan, Wang, Yanfang, Chen, Shaoyun, Leung, Tak Yeung, Cheung, Sau Wai, Kwok, Yvonne K., Morton, Cynthia C., Zhu, Yuanfang, Choy, Kwong Wai
Publicado 2019