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Immediate postpartum cessation of tenofovir did not increase risk of virological or clinical relapse in highly viremic pregnant mothers with chronic hepatitis B infection

JHEP reports, 2024-05, Vol.6 (5), p.101050-101050, Article 101050

2024

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Knowledge, attitude and ethical consideration of Chinese couples requesting preimplantation genetic testing in Hong Kong

The journal of obstetrics and gynaecology research, 2019-06, Vol.45 (6), p.1096-1105

2019

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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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A prenatal case of split-hand malformation associated with 17p13.3 triplication – A dilemma in genetic counseling

European journal of medical genetics, 2014-02, Vol.57 (2), p.81-84

2014

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A newborn with a 790 kb chromosome 17p13.3 microduplication presenting with aortic stenosis, microcephaly and dysmorphic facial features – Is cardiac assessment necessary for all patients with 17p13.3 microduplication?

European journal of medical genetics, 2012-12, Vol.55 (12), p.758-762

2012

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20 years review of antenatal diagnosis of haemoglobin Bart's disease and treatment with intrauterine transfusion

Prenatal diagnosis, 2022-08, Vol.42 (9), p.1155-1161

2022

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Alport’s syndrome: case of a giant esophageal tumor

Esophagus : official journal of the Japan Esophageal Society, 2013-06, Vol.10 (2), p.114-117

2013

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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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Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong

PloS one, 2014-02, Vol.9 (2), p.e87988-e87988

2014

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Noninvasive prenatal molecular karyotyping from maternal plasma

PloS one, 2013-04, Vol.8 (4), p.e60968

2013

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

BMJ, 2011-01, Vol.342 (jan11 1), p.c7401-c7401

2011

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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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Role of microRNAs in embryo–endometrial interactions: biological functions and clinical applications

Reproductive and Developmental Medicine, 2023-12, Vol.7 (4), p.238-251

2023

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Systematic identification of placental epigenetic signatures for the noninvasive prenatal detection of Edwards syndrome

PloS one, 2010-11, Vol.5 (11), p.e15069-e15069

2010

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A Fetus with Hb Bart's Disease Due to Maternal Uniparental Disomy for Chromosome 16

Hemoglobin, 2016-01, Vol.40 (1), p.66-69

2016

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First Report of a Novel Deletion Due to εγδβ-Thalassemia in a Chinese Family

Hemoglobin, 2017-05, Vol.41 (3), p.175-179

2017

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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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Spread of X inactivation on chromosome 15 is associated with a more severe phenotype in a girl with an unbalanced t(X; 15) translocation

American journal of medical genetics. Part A, 2014-10, Vol.164A (10), p.2521-2528

2014

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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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Detection of the S252W mutation in fibroblast growth factor receptor 2 (FGFR2) in fetal DNA from maternal plasma in a pregnancy affected by Apert syndrome

Prenatal diagnosis, 2011-02, Vol.31 (2), p.218-220

2011

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Semi-quantitative fluorescent PCR analysis identifies PRKAA1 on chromosome 5 as a potential candidate cancer gene of cervical cancer

Gynecologic oncology, 2006-10, Vol.103 (1), p.219-225

2006

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

Prenatal diagnosis, 2009-02, Vol.29 (2), p.151-155

2009

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Chromosomal anomalies and Y-microdeletions among Chinese subfertile men in Hong Kong

Hong Kong medical journal = Xianggang yi xue za zhi, 2009-02, Vol.15 (1), p.31-38

2009

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

Hong Kong medical journal = Xianggang yi xue za zhi, 2008-02, Vol.14 (1), p.6-13

2008

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Prenatal findings and delineation of de novo concurrent partial trisomy 7q(7q31.2 → qter) and partial monosomy 6q(6q26 → qter) by high-resolution array CGH

The journal of maternal-fetal & neonatal medicine, 2009-11, Vol.22 (11), p.1014-1020

2009

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Immediate postpartum cessation of tenofovir did not increase risk of virological or clinical relapse in highly viremic pregnant mothers with chronic hepatitis B infection

Knowledge, attitude and ethical consideration of Chinese couples requesting preimplantation genetic testing in Hong Kong

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

A prenatal case of split-hand malformation associated with 17p13.3 triplication – A dilemma in genetic counseling

A newborn with a 790 kb chromosome 17p13.3 microduplication presenting with aortic stenosis, microcephaly and dysmorphic facial features – Is cardiac assessment necessary for all patients with 17p13.3 microduplication?

20 years review of antenatal diagnosis of haemoglobin Bart's disease and treatment with intrauterine transfusion

Alport’s syndrome: case of a giant esophageal tumor

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

Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong

Noninvasive prenatal molecular karyotyping from maternal plasma

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

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

Role of microRNAs in embryo–endometrial interactions: biological functions and clinical applications

Systematic identification of placental epigenetic signatures for the noninvasive prenatal detection of Edwards syndrome

A Fetus with Hb Bart's Disease Due to Maternal Uniparental Disomy for Chromosome 16

First Report of a Novel Deletion Due to εγδβ-Thalassemia in a Chinese Family

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

Spread of X inactivation on chromosome 15 is associated with a more severe phenotype in a girl with an unbalanced t(X; 15) translocation

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

Detection of the S252W mutation in fibroblast growth factor receptor 2 (FGFR2) in fetal DNA from maternal plasma in a pregnancy affected by Apert syndrome

Semi-quantitative fluorescent PCR analysis identifies PRKAA1 on chromosome 5 as a potential candidate cancer gene of cervical cancer

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

Chromosomal anomalies and Y-microdeletions among Chinese subfertile men in Hong Kong

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

Prenatal findings and delineation of de novo concurrent partial trisomy 7q(7q31.2 → qter) and partial monosomy 6q(6q26 → qter) by high-resolution array CGH

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