Noninvasive Prenatal Molecular Karyotyping from Maternal Plasma

por Yu, Stephanie C. Y., Jiang, Peiyong, Choy, Kwong W., Chan, Kwan Chee Allen, Won, Hye-Sung, Leung, Wing C., Lau, Elizabeth T., Tang, Mary H. Y., Leung, Tak Y., Lo, Yuk Ming Dennis, Chiu, Rossa W. K.
Publicado 2013

Systematic Identification of Placental Epigenetic Signatures for the Noninvasive Prenatal Detection of Edwards Syndrome

por Tsui, Dana W. Y., Lam, Y. M. Doris, Lee, Wing S., Leung, Tak Y., Lau, Tze K., Lau, Elizabeth T., Tang, Mary H. Y., Akolekar, Ranjit, Nicolaides, Kypros H., Chiu, Rossa W. K., Lo, Y. M. Dennis, Chim, Stephen S. C.
Publicado 2010

Whole-Genome Array CGH Evaluation for Replacing Prenatal Karyotyping in Hong Kong

por Kan, Anita S. Y., Lau, Elizabeth T., Tang, W. F., Chan, Sario S. Y., Ding, Simon C. K., Chan, Kelvin Y. K., Lee, C. P., Hui, Pui Wah, Chung, Brian H. Y., Leung, K. Y., Ma, Teresa, Leung, Wing C., Tang, Mary H. Y.
Publicado 2014

The Clinical Impact of Chromosomal Microarray on Paediatric Care in Hong Kong

por Tao, Victoria Q., Chan, Kelvin Y. K., Chu, Yoyo W. Y., Mok, Gary T. K., Tan, Tiong Y., Yang, Wanling, Lee, So Lun, Tang, Wing Fai, Tso, Winnie W. Y., Lau, Elizabeth T., Kan, Anita S. Y., Tang, Mary H., Lau, Yu-lung, Chung, Brian H. Y.
Publicado 2014

Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES)

por Leung, Gordon K C, Mak, Christopher C Y, Fung, Jasmine L F, Wong, Wilfred H S, Tsang, Mandy H Y, Yu, Mullin H C, Pei, Steven L C, Yeung, K S, Mok, Gary T K, Lee, C P, Hui, Amelia P W, Tang, Mary H Y, Chan, Kelvin Y K, Liu, Anthony P Y, Yang, Wanling, Sham, P C, Kan, Anita S Y, Chung, Brian H Y
Publicado 2018

Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study

por Chiu, Rossa W K, Akolekar, Ranjit, Zheng, Yama W L, Leung, Tak Y, Sun, Hao, Chan, K C Allen, Lun, Fiona M F, Go, Attie T J I, Lau, Elizabeth T, To, William W K, Leung, Wing C, Tang, Rebecca Y K, Au-Yeung, Sidney K C, Lam, Helena, Kung, Yu Y, Zhang, Xiuqing, van Vugt, John M G, Minekawa, Ryoko, Tang, Mary H Y, Wang, Jun, Oudejans, Cees B M, Lau, Tze K, Nicolaides, Kypros H, Lo, Y M Dennis
Publicado 2011

Noninvasive Prenatal Diagnosis of Fetal Trisomy 18 and Trisomy 13 by Maternal Plasma DNA Sequencing

por Chen, Eric Z., Chiu, Rossa W. K., Sun, Hao, Akolekar, Ranjit, Chan, K. C. Allen, Leung, Tak Y., Jiang, Peiyong, Zheng, Yama W. L., Lun, Fiona M. F., Chan, Lisa Y. S., Jin, Yongjie, Go, Attie T. J. I., Lau, Elizabeth T., To, William W. K., Leung, Wing C., Tang, Rebecca Y. K., Au-Yeung, Sidney K. C., Lam, Helena, Kung, Yu Y., Zhang, Xiuqing, van Vugt, John M. G., Minekawa, Ryoko, Tang, Mary H. Y., Wang, Jun, Oudejans, Cees B. M., Lau, Tze K., Nicolaides, Kypros H., Lo, Y. M. Dennis
Publicado 2011