Zobrazeno 1 - 10
of 334
pro vyhledávání: '"Tze Kin, Lau"'
Autor:
Vivian Kwun Sin Ng, Tze Kin Lau, Anita Sik Yau Kan, Brian Hon Yin Chung, Ho Ming Luk, Wai Fu Ng, Mengmeng Shi, Kwong Wai Choy, Ye Cao, Wing Cheong Leung
Publikováno v:
Diagnostics, Vol 11, Iss 9, p 1576 (2021)
Microcephaly and microphthalmia are both rare congenital abnormalities, while concurrently, these two are even rarer. The underlying etiology would be complex interplaying between heterogeneous genetic background and the environmental pathogens, part
Externí odkaz:
https://doaj.org/article/6331da45a83a44b3b5ad220aa82fb52c
Autor:
Tze Kin Lau, Tak Yeung Leung, Sunny Wai Hung Cheung, Matthew Hoi Kin Chau, Kwong Wai Choy, Yuen Ha Ting, Yvonne K. Kwok, Doris Yuk Man Lam, Wan Pang Chan, Mengmeng Shi, Xiaofan Zhu, Yves Ville
Publikováno v:
Prenatal Diagnosis. 40:1005-1012
OBJECTIVE To report genome-wide cell-free DNA (cfDNA) screening facilitating the diagnosis of Pallister-Killian syndrome (PKS). METHODS This is a retrospective cohort analysis of positive genome-wide cfDNA screening results showing increased signal f
Publikováno v:
Journal of Fetal Medicine. :17-23
Abstract No single invention in the past has created such a rapid and massive impact on clinical obstetric practice as the introduction of noninvasive prenatal screening (NIPS) for chromosomal abnormalities using cell-free DNA in maternal plasma. How
Autor:
Olivia Yiu Man Chan, Tze-Kin Lau
Publikováno v:
Hong Kong Journal of Gynaecology, Obstetrics and Midwifery. 20:48-52
Autor:
Shan Dan, Fang Chen, Kwong Wai Choy, Fuman Jiang, Jingrong Lin, Zhaoling Xuan, Wei Wang, Shengpei Chen, Xuchao Li, Hui Jiang, Tak Yeung Leung, Tze Kin Lau, Yue Su, Weiyuan Zhang, Xiuqing Zhang
Publikováno v:
PLoS ONE, Vol 7, Iss 2, p e27835 (2012)
Fetal chromosomal abnormalities are the most common reasons for invasive prenatal testing. Currently, G-band karyotyping and several molecular genetic methods have been established for diagnosis of chromosomal abnormalities. Although these testing me
Externí odkaz:
https://doaj.org/article/14239b72586b46d39ba27a0b0717d209
Autor:
Brian H.Y. Chung, Wai Fu Ng, Anita Sik Yau Kan, Ye Cao, Tze Kin Lau, Mengmeng Shi, Wing Cheong Leung, Kwong Wai Choy, Vivian Kwun Sin Ng, Ho Ming Luk
Publikováno v:
Diagnostics
Diagnostics, Vol 11, Iss 1576, p 1576 (2021)
Diagnostics, Vol 11, Iss 1576, p 1576 (2021)
Microcephaly and microphthalmia are both rare congenital abnormalities, while concurrently, these two are even rarer. The underlying etiology would be complex interplaying between heterogeneous genetic background and the environmental pathogens, part
Autor:
Shuk Ching Chong, Yu Zheng, Mengmeng Shi, Angeline Linna Liauw, Kwong Wai Choy, Steve Tong, Tze Kin Lau, Ye Cao, Tak Yeung Leung, Jacqueline Pui Wah Chung
Publikováno v:
Genes
Volume 12
Issue 4
Genes, Vol 12, Iss 496, p 496 (2021)
Volume 12
Issue 4
Genes, Vol 12, Iss 496, p 496 (2021)
Demands for expanded carrier screening (ECS) are growing and ECS is becoming an important part of obstetrics practice and reproductive planning. The aim of this study is to evaluate the feasibility of a small-size ECS panel in clinical implementation
Autor:
Tze Kin Lau, Yuen Ha Ting, Yvonne Kwun Yue Cheng, Tak Yeung Leung, Terence T. Lao, Kwok Ming Law
Publikováno v:
Fetal Diagnosis and Therapy. 40:67-72
Pseudoamniotic band syndrome (PABS) is a rare iatrogenic complication that arises after invasive procedures in monochorionic twins. We report 3 cases of PABS, 2 after fetoscopic laser photocoagulation and 1 after bipolar cord coagulation. Two cases w
Autor:
Wai Lam Lau, Yat-Yin Lam, Wing Cheong Leung, M. H. Y. Tang, Kelvin Y.K. Chan, Anita Kan, Tsz-Kin Lo, Tze Kin Lau, Elizabeth T. Lau
Publikováno v:
Journal of Obstetrics and Gynaecology. 37:113-115
Uniparental disomy (UPD) refers to the genetic phenomenon in which both homologous chromosomes are inherited from the same parent, either maternal or paternal. The UPD phenotype is chromosome speci...
Autor:
Yi Zhou, Xiaoling Guo, Tze Kin Lau, Min Chen, Qiufang Liu, Wei Wang, Shengpei Chen, Xuan Huang, Chenming Xu, Shuqiong Shi, Qichang Wu, Hui Jiang, Jing Zheng, Qun Fang, Yangyu Zhao, Xiaomei Shi, Fang Chen, Xiaoyu Pan, Fuman Jiang, Ya Gao, Dongzhu Lei, Yuan Wei, Lifu Liu, Fengxia Su, Huijuan Ge, Xuchao Li, Weiwei Xie, Chunlei Zhang, Hongyun Zhang
Publikováno v:
Prenatal Diagnosis. 34:335-340
Objective The objective of this study is to assess the performance of noninvasive prenatal testing for trisomies 21 and 18 on the basis of massively parallel sequencing of cell-free DNA from maternal plasma in twin pregnancies. Method A double-blind