M. Tang

发表

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

E. Lau, K. Y. Chan, A. Kan, 2014, PloS one.

Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder—implications of a copy number variation involving DPP10

S. Scherer, C. Marshall, V. Wong, 2017, Molecular Autism.

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.

Rapid aneuploidy screening (FISH or QF-PCR): the changing scene in prenatal diagnosis?

E. Lau, W. Leung, M. Tang, 2004, Expert review of molecular diagnostics.

Haemoglobin level, proportion of haemoglobin Bart's and haemoglobin Portland in fetuses affected by homozygous α0‐thalassemia from 12 to 40 weeks' gestation

M. Tang, T. Li, K. Leung, 2010, Prenatal diagnosis.

Ultrasonographic prediction of homozygous α0‐thalassemia using placental thickness, fetal cardiothoracic ratio and middle cerebral artery Doppler: alone or in combination?

V. Chan, C. P. Lee, M. Tang, 2010, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Ultrasound evaluation of pregnancies at risk for homozygous alpha-thalassaemia-1.

T. Chan, V. Chan, M. Tang, 1987, Prenatal diagnosis.

Ultrasound measurement of placental thickness to detect pregnancies affected by homozygous α-thalassaemia-1

M. Tang, E. Fung, Y. Lam, 1994, The Lancet.

Early ultrasound prediction of pregnancies affected by homozygous alpha-thalassaemia-1.

C. P. Lee, M. Tang, Y. Lam, 1997, Prenatal diagnosis.

Second-trimester hydrops fetalis in pregnancies affected by homozygous alpha-thalassaemia-1.

C. P. Lee, M. Tang, Y. Lam, 1997, Prenatal diagnosis.

Limb reduction defects in fetuses with homozygous alpha-thalassaemia-1.

C. P. Lee, M. Tang, Y. Lam, 1997, Prenatal diagnosis.

PRENATAL DIAGNOSIS OF HAEMOGLOBIN BART'S DISEASE BY CORDOCENTESIS AT 12–14 WEEKS' GESTATION

M. Tang, Y. Lam, M. Tang, 1997, Prenatal diagnosis.

Serologic Characteristics and Clinical Significance of Miltenberger Antibodies among Chinese Patients in Hong Kong

M. Tang, T. Lao, K. Mak, 1998, Vox sanguinis.

First trimester fetal biparietal diameter and head circumference in Chinese population

Chin-peng Lee, Ommega Internationals, M. Tang, 2017 .

First‐trimester ultrasound diagnosis of holoprosencephaly: three case reports

H. Wong, M. Tang, L. Ng, 1999, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Comparison of nuchal and detailed morphology ultrasound examinations in early pregnancy for fetal structural abnormality screening: a randomized controlled trial

M. Chen, C. P. Lee, M. Tang, 2008, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Human Chorionic Gonadotropin and Plasma Protein-A in Alpha0-Thalassemia Pregnancies

E. Lau, Chin-peng Lee, K. Leung, 2006, Obstetrics and gynecology.

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

E. Lau, A. Kan, B. Chung, 2014, American journal of medical genetics. Part A.

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

Y. Lau, G. T. K. Mok, W. Tang, 2014, PloS one.

Title The clinical impact of chromosomal microarray on paediatriccare in Hong Kong

Y. Lau, G. T. K. Mok, W. Tang, 2014 .

Title Comparative gene expression analysis of the human periodontal ligament in deciduous and permanent teeth

Y. Lau, G. T. K. Mok, W. Tang, 2014 .

Paternal uniparental disomy of chromosome 19 in a pair of monochorionic diamniotic twins with dysmorphic features and developmental delay

S. Scherer, R. Pfundt, C. Marshall, 2018, Journal of Medical Genetics.

Prenatal sonographic diagnosis of conjoined twins in the first trimester: two case reports

C. P. Lee, M. Tang, C. Lam, 1998, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

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.

Outcome of twin pregnancies after amniocentesis

A. Kan, Chin-peng Lee, K. Leung, 2012, The journal of obstetrics and gynaecology research.

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

Y. Cheng, T. Leung, K. Y. Chan, 2017, Hemoglobin.

Simultaneous pulsed Doppler velocimetry of fetal aorta and inferior vena cava. Diagnosis of fetal congenital heart block; two case reports.

F. Chan, M. Tang, C. Lam, 1990, European journal of obstetrics, gynecology, and reproductive biology.

Prenatal ultrasonographic prediction of homozygous type 1 alpha-thalassemia at 12 to 13 weeks of gestation.

C. P. Lee, M. Tang, H. Tse, 1999, American journal of obstetrics and gynecology.

Cystic hygroma detected in the first trimester scan in Hong Kong

Chin-peng Lee, M. Tang, R. Tang, 2014, 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.

Sonographic features of lethal multiple pterygium syndrome at 14 weeks

Chin-peng Lee, M. Tang, G. Chan, 2005, Prenatal diagnosis.

Outcome and management of babies with prenatal ultrasonographic renal abnormalities.

M. Tang, B. Lam, A. Ghosh, 1993, American journal of perinatology.

Maternal serum alpha-fetoprotein and human chorionic gonadotrophin in pregnancies conceived after intracytoplasmic sperm injection and conventional in-vitro fertilization.

W. Yeung, P. Ho, E. Ng, 1999, Human reproduction.

Are herbal medicinal products less teratogenic than Western pharmaceutical products.

Chin-peng Lee, K. Leung, M. Tang, 2002, Acta pharmacologica Sinica.

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

A. Kan, E. Ng, Chin-peng Lee, 2020, Frontiers in Genetics.

Middle cerebral artery Doppler study in fetuses with homozygous alpha-thalassaemia-1 at 12-13 weeks of gestation.

M. Tang, Y. Lam, 2002, Prenatal diagnosis.

Maternal plasma or human serum albumin in wash buffer enhances enrichment and ex vivo expansion of human umbilical cord blood CD34+ cells

Y. Lau, E. Lau, M. Tang, 2007, British journal of haematology.

Attitude of at‐risk subjects towards preimplantation genetic diagnosis of α‐ and β‐thalassaemias in Hong Kong

W. Yeung, P. Ho, E. Ng, 2002 .

Attitude of at-risk subjects towards preimplantation genetic diagnosis of alpha- and beta-thalassaemias in Hong Kong.

W. Yeung, P. Ho, E. Ng, 2002, Prenatal diagnosis.

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

A. Kan, Chin-peng Lee, P. Hui, 2017, Archives of Gynecology and Obstetrics.

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

E. Lau, K. Y. Chan, A. Kan, 2014, European journal of medical genetics.

Ultrasound screening of fetal structural abnormalities at 12 to 14 weeks in Hong Kong

Chin-peng Lee, M. Tang, Y. Lam, 2004, Prenatal diagnosis.

Justification of maternal serum alphafetoprotein screening in a population with low incidence of neural tube defects

M. Tang, H. Ma, A. Ghosh, 1986, Prenatal diagnosis.

Prenatal Diagnosis of Congenital Fetal Arrhythmias by Simultaneous Pulsed Doppler Velocimetry of the Fetal Abdominal Aorta and Inferior Vena Cava

F. Chan, M. Tang, C. Lam, 1990, Obstetrics and gynecology.

Characterization of a novel mutation in F8 gene causing severe haemophilia A by deletion mapping with STS markers

E. Lau, P. Au, C. Lin, 2015, Haemophilia : the official journal of the World Federation of Hemophilia.

Biochemical hypothyroidism--a new finding in mirror syndrome?

W. Leung, M. Tang, T. Lao, 2006, European journal of obstetrics, gynecology, and reproductive biology.

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

H. Ngan, A. Cheung, E. Lau, 2006, Gynecologic oncology.

Thermocoagulation of fetal sacrococcygeal teratoma.

M. Tang, T. Shek, Y. Lam, 2002, Prenatal diagnosis.

Factors affecting outcomes of prenatally‐diagnosed tumours

P. Tam, K. Chan, C. P. Lee, 2002, Prenatal diagnosis.

Pre-implantation genetic diagnosis in Hong Kong.

P. Ho, W. Yeung, M. Tang, 2003, Hong Kong medical journal = Xianggang yi xue za zhi.

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

E. Lau, P. Ho, W. Yeung, 2009, Hong Kong medical journal = Xianggang yi xue za zhi.

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

Peiyong Jiang, Yama W. L. Zheng, Tak Y. Leung, 2011, PloS one.

Prenatal detection of a de novo Yqh-acrocentric translocation.

E. Lau, M. Tang, L. Ng, 2006, Clinical biochemistry.

Prenatal Screening for Thalassemias

P. Au, K. Leung, M. Tang, 2020 .

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

Yama W. L. Zheng, Xiuqing Zhang, K. Nicolaides, 2011, BMJ : British Medical Journal.

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

K. Y. Chan, A. Kan, B. Chung, 2019, American journal of medical genetics. Part C, Seminars in medical genetics.

Title Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving

S. Scherer, C. Marshall, V. Wong, 2017 .

Diagnostic yield of array CGH in patients with autism spectrum disorder in Hong Kong

K. Kwong, W. Tang, E. Lau, 2016, Clinical and Translational Medicine.

Genetic abnormalities and HPV status in cervical and vulvar squamous cell carcinomas.

H. Ngan, E. Lau, M. Tang, 2005, Cancer genetics and cytogenetics.

Prenatal diagnosis of agenesis of the corpus callosum and cerebellar vermian hypoplasia associated with a microdeletion on chromosome 1p32

E. Lau, B. Chung, Simon C. K. Ding, 2013 .

A fetus coexisting with a complete hydatidiform mole with trisomy 9 of maternal origin

M. Pertile, E. Lau, A. Kan, 2018, The journal of obstetrics and gynaecology research.

Can Amnio–Polymerase Chain Reaction Alone Replace Conventional Cytogenetic Study for Women With Positive Biochemical Screening for Fetal Down Syndrome?

E. Lau, W. Leung, M. Tang, 2003, Obstetrics and gynecology.

The Effect of Volume of Chorionic Villi on Long-Term Cell Culture

E. Lau, Chin-peng Lee, M. Tang, 2008, Fetal Diagnosis and Therapy.

Recurrent congenital chylothorax

M. Tang, A. Ghosh, P. King, 1991, Prenatal diagnosis.

Management and outcome of antenatally diagnosed congenital cystic adenomatoid malformation of the lung.

M. Tang, B. Lam, N. Tsoi, 2007, Hong Kong medical journal = Xianggang yi xue za zhi.

Variable levels of mosaicism for trisomy 21 in a non‐immune hydropic infant with chylothorax

M. Tang, B. Lam, Y. Lam, 1999, Prenatal diagnosis.

Echogenic bowel in fetuses with homozygous α‐thalassemia‐1 in the first and second trimesters

C. P. Lee, M. Tang, H. Tse, 1999 .

Echogenic bowel in fetuses with homozygous alpha-thalassemia-1 in the first and second trimesters.

C. P. Lee, M. Tang, H. Tse, 1999, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Nuchal translucency in pregnancies conceived after assisted reproduction technology

P. Ho, Chin-peng Lee, P. Hui, 2006, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Nuchal translucency in pregnancies conceived after assisted reproduction technology

P. Ho, W. Yeung, P. Hui, 2005, Current opinion in obstetrics & gynecology.

Prenatal diagnosis of haemoglobin Bart's disease by cordocentesis at 12-14 weeks--experience with the first 59 cases.

M. Tang, Y. Lam, 2000, Prenatal diagnosis.

Factors associated with common and atypical chromosome abnormalities after positive combined first-trimester screening in Chinese women: a retrospective cohort study

K. Leung, T. Ma, M. Tang, 2019, BMC Pregnancy and Childbirth.

Noninvasive Prenatal Molecular Karyotyping from Maternal Plasma

K. Choy, H. Won, P. Jiang, 2013, PloS one.

Prenatal evaluation of facial clefts by three‐dimensional extended imaging

M. Tang, K. Leung, L. Wang, 2007, Prenatal diagnosis.

Sonographic diagnosis of congenital megalourethra at 13 weeks of gestation

M. Tang, Y. Lam, 2000, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

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

E. Lau, K. Y. Chan, A. Kan, 2016, Hemoglobin.

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

K. Choy, T. Leung, T. Lau, 2009, 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.

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

D. Tsui, K. Nicolaides, T. Leung, 2010, PloS one.

Cardiac blood flow studies in fetuses with haemoglobin bart's disease

M. Tang, M. Leung, A. Ghosh, 1994, Prenatal Diagnosis.

Alport’s syndrome: case of a giant esophageal tumor

S. Law, E. Lau, B. Chung, 2012, Esophagus.

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?

E. Lau, K. Y. Chan, B. Chung, 2012, European journal of medical genetics.

Prenatal diagnosis of congenital heart malformations: classification based on abnormalities detected by the four‐chamber view

M. Tang, M. Leung, A. Ghosh, 1999, Prenatal diagnosis.

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

P. Sham, B. Chung, Wanling Yang, 2018, BMC Medical Genomics.

The risk of alpha-thalassaemia in offspring of beta-thalassaemia carriers in Hong Kong.

M. Tang, Y. Lam, V. Chan, 1997, Prenatal diagnosis.

Effectiveness of a Technology-Based Injury Prevention Program for Enhancing Mothers’ Knowledge of Child Safety: Protocol for a Randomized Controlled Trial

C. Or, P. Ip, K. Chan, 2016, JMIR research protocols.

Prenatal diagnosis and long‐term follow‐up of a Chinese patient with mosaic variegated aneuploidy and its molecular analysis

K. Y. Chan, A. Kan, W. Leung, 2020, Clinical case reports.

Histological findings in a case of alobar holoprosencephaly diagnosed at 10 weeks of pregnancy

H. Wong, M. Tang, K. Yan, 1999, Prenatal diagnosis.

Sonographic visualization of fetal fingers and toes at 10 weeks of gestation.

M. Tang, Y. Lam, 2002 .

Maternal serum hCG and alpha-fetoprotein levels in pregnancies conceived after IVF or ICSI with fresh and frozen-thawed embryos.

P. Ho, W. Yeung, P. Hui, 2003, Human reproduction.

The effect of fetal gender on second-trimester maternal serum inhibin-A concentration.

M. Tang, Y. Lam, 2001, Prenatal diagnosis.

Comparison of inter‐ and intraobserver agreement between three types of fetal volume measurement technique (XI VOCAL™, VOCAL™ and multiplanar)

M. Tang, K. B. Cheong, K. Y. Leung, 2009, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Nuchal translucency in dichorionic twins conceived after assisted reproduction

E. Ng, W. Yeung, E. Ng, 2006, Prenatal diagnosis.

Nuchal translucency in fetuses affected by homozygous α‐thalassemia‐1 at 12–13 weeks of gestation

C. P. Lee, M. Tang, H. Tse, 1999, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Molecular basis of von Hippel-Lindau syndrome in Chinese patients.

W. So, C. Chow, C. Lam, 2011, Chinese medical journal.

Intrauterine therapy in a fetus with congenital dyserythropoietic anaemia type I

M. Chen, M. Tang, K. Y. Wong, 2014, Journal of Obstetrics and Gynaecology Research.

Cost-effectiveness analysis of chromosomal microarray as a primary test for prenatal diagnosis in Hong Kong

K. Y. Chan, A. Kan, B. Chung, 2020, BMC Pregnancy and Childbirth.

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

P. Sham, K. Y. Chan, A. Kan, 2018, BMC Medical Genomics.

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

Yama W. L. Zheng, Xiuqing Zhang, K. Nicolaides, 2011, BMJ : British Medical Journal.

Monozygotic Dichorionic Twins Heterokaryotypic for Duplication Chromosome 2q13-q23.3

K. Choy, E. Lau, W. Leung, 2009, Fetal Diagnosis and Therapy.

Mosaic partial trisomy 17q2.

M. Tang, A. Ghosh, P. King, 1991, Journal of Medical Genetics.

Mosaic partial trisomy 17 q 2

M. Tang, A. Ghosh, P. King, 2022 .

Is there an optimal gestation for ultrasound examination of fetal nasal bone in the first trimester?

Chin-peng Lee, P. Hui, W. Leung, 2004, Prenatal diagnosis.