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Human placental exosomes induce maternal systemic immune tolerance by reprogramming circulating monocytes

Journal of nanobiotechnology, 2022-02, Vol.20 (1), p.86-86, Article 86

2022

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Experience of chromosomal microarray applied in prenatal and postnatal settings in Hong Kong

American journal of medical genetics. Part C, Seminars in medical genetics, 2019-06, Vol.181 (2), p.196-207

2019

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Dysregulation of the CD147 complex confers defective placental development: A pathogenesis of early‐onset preeclampsia

Clinical and translational medicine, 2022-06, Vol.12 (6), p.e826-n/a

2022

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Prenatal diagnosis of 5p deletion syndrome: Report of five cases

The journal of obstetrics and gynaecology research, 2019-04, Vol.45 (4), p.923-926

2019

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

BMC medical genomics, 2018-10, Vol.11 (1), p.93-93, Article 93

2018

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Prenatal presentation in two fetuses with features of Beckwith Wiedemann syndrome—An unexpected diagnosis of androgenetic chimera and its clinical implications

American journal of medical genetics. Part A, 2022-05, Vol.188 (5), p.1562-1567

2022

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Increasing prenatal diagnosis of chimeras with the use of noninvasive prenatal screening: Report of two cases

Prenatal diagnosis, 2021-05, Vol.41 (6), p.697-700

2021

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Optimal timing of hepatitis B virus DNA quantification and clinical predictors for higher viral load during pregnancy

Acta obstetricia et gynecologica Scandinavica, 2019-10, Vol.98 (10), p.1301-1306

2019

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Implementation of Public Funded Genome Sequencing in Evaluation of Fetal Structural Anomalies

Genes, 2022-11, Vol.13 (11), p.2088

2022

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Expanded Carrier Screening in Chinese Population - A Survey on Views and Acceptance of Pregnant and Non-Pregnant Women

Frontiers in genetics, 2020-11, Vol.11, p.594091-594091

2020

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Decision outcomes in women offered noninvasive prenatal test (NIPT) for positive Down screening results

The journal of maternal-fetal & neonatal medicine, 2019-01, Vol.32 (2), p.348-350

2019

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Informed choice and decision making in women offered cell‐free DNA prenatal genetic screening

Prenatal diagnosis, 2017-03, Vol.37 (3), p.299-302

2017

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The KLHL40 c.1516A>C is a Chinese‐specific founder mutation causing nemaline myopathy 8: Report of six patients with pre‐ and postnatal phenotypes

Molecular genetics & genomic medicine, 2020-07, Vol.8 (7), p.e1229-n/a

2020

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A case of prenatal isolated talipes and 22q11.2 deletion syndrome—an important chromosomal disorder missed by noninvasive prenatal screening

Prenatal diagnosis, 2018-04, Vol.38 (5), p.376-378

2018

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A prospective randomized comparison of sublingual and oral misoprostol when combined with mifepristone for medical abortion at 12–20 weeks gestation

Human reproduction (Oxford), 2005-11, Vol.20 (11), p.3062-3066

2005

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Study of the extent of information desired by women undergoing non‐invasive prenatal testing following positive prenatal Down‐syndrome screening test results

International journal of gynecology and obstetrics, 2017-06, Vol.137 (3), p.338-339

2017

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Parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong

The journal of obstetrics and gynaecology research, 2017-12, Vol.43 (12), p.1821-1829

2017

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

Diagnostics (Basel), 2021-09, Vol.11 (9), p.1576

2021

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Application of Prenatal Whole Exome Sequencing for Structural Congenital Anomalies-Experience from a Local Prenatal Diagnostic Laboratory

Healthcare (Basel), 2022-12, Vol.10 (12), p.2521

2022

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Bridging the gap from prenatal karyotyping to whole-genome array comparative genomic hybridization in Hong Kong: survey on knowledge and acceptance of health-care providers and pregnant women

Archives of gynecology and obstetrics, 2017-12, Vol.296 (6), p.1109-1116

2017

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Effect of non-invasive prenatal testing as a contingent approach on the indications for invasive prenatal diagnosis and prenatal detection rate of Down's syndrome

Hong Kong medical journal = Xianggang yi xue za zhi, 2016-06, Vol.22 (3), p.223-230

2016

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Effect of knowledge on women’s likely uptake of and willingness to pay for non-invasive test (NIPT)

European journal of obstetrics & gynecology and reproductive biology, 2018-03, Vol.222, p.183-184

2018

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Pregnancy-associated plasma protein A for prediction of fetal growth restriction

International journal of gynecology and obstetrics, 2015-08, Vol.130 (2), p.200-200

2015

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The case for routine Gram stain following invasive prenatal procedures with retained intrauterine device

Journal of obstetrics and gynaecology, 2019-01, Vol.39 (1), p.129-130

2019

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An Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Krüppel-like Factor 1 mutations

Hemoglobin, 2016-11, Vol.40 (6), p.431-434

2016

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Human placental exosomes induce maternal systemic immune tolerance by reprogramming circulating monocytes

Experience of chromosomal microarray applied in prenatal and postnatal settings in Hong Kong

Dysregulation of the CD147 complex confers defective placental development: A pathogenesis of early‐onset preeclampsia

Prenatal diagnosis of 5p deletion syndrome: Report of five cases

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

Prenatal presentation in two fetuses with features of Beckwith Wiedemann syndrome—An unexpected diagnosis of androgenetic chimera and its clinical implications

Increasing prenatal diagnosis of chimeras with the use of noninvasive prenatal screening: Report of two cases

Optimal timing of hepatitis B virus DNA quantification and clinical predictors for higher viral load during pregnancy

Implementation of Public Funded Genome Sequencing in Evaluation of Fetal Structural Anomalies

Expanded Carrier Screening in Chinese Population - A Survey on Views and Acceptance of Pregnant and Non-Pregnant Women

Decision outcomes in women offered noninvasive prenatal test (NIPT) for positive Down screening results

Informed choice and decision making in women offered cell‐free DNA prenatal genetic screening

The KLHL40 c.1516A>C is a Chinese‐specific founder mutation causing nemaline myopathy 8: Report of six patients with pre‐ and postnatal phenotypes

A case of prenatal isolated talipes and 22q11.2 deletion syndrome—an important chromosomal disorder missed by noninvasive prenatal screening

A prospective randomized comparison of sublingual and oral misoprostol when combined with mifepristone for medical abortion at 12–20 weeks gestation

Study of the extent of information desired by women undergoing non‐invasive prenatal testing following positive prenatal Down‐syndrome screening test results

Parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong

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

Application of Prenatal Whole Exome Sequencing for Structural Congenital Anomalies-Experience from a Local Prenatal Diagnostic Laboratory

Bridging the gap from prenatal karyotyping to whole-genome array comparative genomic hybridization in Hong Kong: survey on knowledge and acceptance of health-care providers and pregnant women

Effect of non-invasive prenatal testing as a contingent approach on the indications for invasive prenatal diagnosis and prenatal detection rate of Down's syndrome

Effect of knowledge on women’s likely uptake of and willingness to pay for non-invasive test (NIPT)

Pregnancy-associated plasma protein A for prediction of fetal growth restriction

The case for routine Gram stain following invasive prenatal procedures with retained intrauterine device

An Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Krüppel-like Factor 1 mutations

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