T. K. Lau

The impact of human copy number variation on a new era of genetic testing

K. Choy, S. Setlur, C. Lee, 2010, BJOG : an international journal of obstetrics and gynaecology.

Rapid aneuploidy testing (knowing less) versus traditional karyotyping (knowing more) for advanced maternal age: what would be missed, who should decide?

E. Lau, W. Leung, M. Tang, 2008, Hong Kong medical journal = Xianggang yi xue za zhi.

Two IUGR foetuses with maternal uniparental disomy of chromosome 6 or UPD(6)mat

E. Lau, A. Kan, W. Leung, 2017, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.

Noninvasive prenatal testing of trisomies 21 and 18 by massively parallel sequencing of maternal plasma DNA in twin pregnancies

Hui Jiang, Yuan Wei, Yangyu Zhao, 2014, Prenatal diagnosis.

Fetal aneuploidy screening by maternal plasma DNA sequencing: ‘False positive’ due to confined placental mosaicism

H. Zhang, Wei Wang, Hongyun Zhang, 2013, Prenatal diagnosis.

Assessing discrepant findings between QF‐PCR on uncultured prenatal samples and karyotyping on long‐term culture

E. Lau, W. Leung, T. K. Lau, 2009, Prenatal diagnosis.

Discordant results between fetal karyotyping and non‐invasive prenatal testing by maternal plasma sequencing in a case of uniparental disomy 21 due to trisomic rescue

C. Liao, Dongzhi Li, M. Pan, 2013, Prenatal diagnosis.

Secondary findings from non‐invasive prenatal testing for common fetal aneuploidies by whole genome sequencing as a clinical service

K. Choy, Wei Wang, T. Lau, 2013, Prenatal diagnosis.

Clinical application of massively parallel sequencing‐based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11 105 pregnancies with mixed risk factors

Jian Wang, Songgang Li, Xiuqing Zhang, 2012, Prenatal diagnosis.

Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center

S. Cheung, H. Zhang, K. Choy, 2014 .

Non-invasive prenatal screening of fetal sex chromosomal abnormalities: perspective of pregnant women

T. Lau, R. Pooh, T. K. Lau, 2012, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

A Fetus with Congenital Microcephaly, Microphthalmia and Cataract Was Detected with Biallelic Variants in the OCLN Gene: A Case Report

K. Choy, A. Kan, B. Chung, 2021, Diagnostics.