Noninvasive prenatal molecular karyotyping from maternal plasma
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
Published in PloS one (17.04.2013)
Published in PloS one (17.04.2013)
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Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong
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
Published in PloS one (05.02.2014)
Published in PloS one (05.02.2014)
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The clinical impact of chromosomal microarray on paediatric care in Hong Kong
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
Published in PloS one (15.10.2014)
Published in PloS one (15.10.2014)
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Direct purification and immobilization of his-tagged enzymes using unmodified nickel ferrite NiFe2O4 magnetic nanoparticles
Lau, Elizabeth C. H. T., Dodds, Kimberley C., McKenna, Catherine, Cowan, Rhona M., Ganin, Alexey Y., Campopiano, Dominic J., Yiu, Humphrey H. P.
Published in Scientific reports (06.12.2023)
Published in Scientific reports (06.12.2023)
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Systematic identification of placental epigenetic signatures for the noninvasive prenatal detection of Edwards syndrome
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
Published in PloS one (30.11.2010)
Published in PloS one (30.11.2010)
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Noninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencing
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
Published in PloS one (06.07.2011)
Published in PloS one (06.07.2011)
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Alport’s syndrome: case of a giant esophageal tumor
Tsang, Julian S., Tong, Daniel K. H., Chung, Brian H. Y., Tang, Mary H. Y., Lau, Elizabeth T., Chan, Godfrey C. F., Law, Simon Y. K.
Published in Esophagus : official journal of the Japan Esophageal Society (01.06.2013)
Published in Esophagus : official journal of the Japan Esophageal Society (01.06.2013)
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Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study
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
Published in BMJ (11.01.2011)
Published in BMJ (11.01.2011)
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Two IUGR foetuses with maternal uniparental disomy of chromosome 6 or UPD(6)mat
Leung, Wing Cheong, Lau, Wai Lam, Lo, T K, Lau, Tze Kin, Lam, Y Y, Kan, Anita, Chan, Kelvin, Lau, Elizabeth T, Tang, Mary H
Published in Journal of obstetrics and gynaecology (01.01.2017)
Published in Journal of obstetrics and gynaecology (01.01.2017)
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The effect of fast reporting by amnio-PCR on anxiety levels in women with positive biochemical screening for Down syndrome - a randomized controlled trial
Cheong Leung, Wing, Hang Lam, Yung, Wong, Ying, T. Lau, Elizabeth, Hoi Yin Tang, Mary
Published in Prenatal diagnosis (01.03.2002)
Published in Prenatal diagnosis (01.03.2002)
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Localization of Coated Iron Oxide (Fe3O4) Nanoparticles on Tomato Seeds and Their Effects on Growth
Lau, Elizabeth C. H. T, Carvalho, Lucas B, Pereira, Anderson E. S, Montanha, Gabriel S, Corrêa, Camila G, Carvalho, Hudson W. P, Ganin, Alexey Y, Fraceto, Leonardo F, Yiu, Humphrey H. P
Published in ACS applied bio materials (20.07.2020)
Published in ACS applied bio materials (20.07.2020)
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Gold-iron oxide (Au/Fe 3 O 4 ) magnetic nanoparticles as the nanoplatform for binding of bioactive molecules through self-assembly
Lau, Elizabeth C H T, Åhlén, Michelle, Cheung, Ocean, Ganin, Alexey Y, Smith, David G E, Yiu, Humphrey H P
Published in Frontiers in molecular biosciences (2023)
Published in Frontiers in molecular biosciences (2023)
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Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: Implications in transitional care
Liu, Anthony P.Y, Chow, Pak-Cheong, Lee, Pamela P.W, Mok, Gary T.K, Tang, Wing-Fai, Lau, Elizabeth T, Lam, Stephen T.S, Chan, Kelvin Y, Kan, Anita S.Y, Chau, Adolphus K.T, Cheung, Yiu-Fai, Lau, Yu-Lung, Chung, Brian H.Y
Published in European journal of medical genetics (01.05.2014)
Published in European journal of medical genetics (01.05.2014)
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A Fetus with Hb Bart's Disease Due to Maternal Uniparental Disomy for Chromosome 16
Au, Patrick K.C., Kan, Anita S.Y., Tang, Mary H.Y., Leung, Kwok Y., Chan, Kelvin Y.K., Tang, Tommy W.F., Lau, Elizabeth T.
Published in Hemoglobin (02.01.2016)
Published in Hemoglobin (02.01.2016)
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Antibacterial Activities of Ga(III) against E. coli Are Substantially Impacted by Fe(III) Uptake Systems and Multidrug Resistance in Combination with Oxygen Levels
Neill, Christopher J, Harris, Susan, Goldstone, Robert J, Lau, Elizabeth C. H. T, Henry, Theodore B, Yiu, Humphrey H. P, Smith, David G. E
Published in ACS infectious diseases (13.11.2020)
Published in ACS infectious diseases (13.11.2020)
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Two Unusual Cases of Haemoglobin Bart's Hydrops Fetalis due to Uniparental Disomy or Non-Paternity
Kou, K.O., Lee, Helena, Lau, Betty, Wong, W.S., Kan, Anita, Tang, Mary, Lau, Elizabeth T., Poon, C.F., Leung, K.Y.
Published in Fetal diagnosis and therapy (01.01.2014)
Published in Fetal diagnosis and therapy (01.01.2014)
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Expanded Prader-Willi syndrome due to chromosome 15q11.2-14 deletion: Report and a review of literature
Liu, Anthony P.Y., Tang, Wing Fai, Lau, Elizabeth T., Chan, Kelvin Y.K., Kan, Anita S.Y., Wong, Kar Yin, Tso, Winnie W.Y., Jalal, Khair, Lee, So Lun, Chau, Christy S.K., Chung, Brian H.Y.
Published in American journal of medical genetics. Part A (01.06.2013)
Published in American journal of medical genetics. Part A (01.06.2013)
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Spread of X inactivation on chromosome 15 is associated with a more severe phenotype in a girl with an unbalanced t(X; 15) translocation
Yeung, KS, Chee, YY, Luk, HM, Kan, Anita SY, Tang, Mary HY, Lau, Elizabeth T, Shuen, Andrew Y, Lo, Ivan FM, Chan, Kelvin YK, Chung, Brian HY
Published in American journal of medical genetics. Part A (01.10.2014)
Published in American journal of medical genetics. Part A (01.10.2014)
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