Jing Wu

发表

Prenatal diagnosis of fetal right ventricular diverticulum with massive pericardial effusion in one of monochorionic diamniotic twins: a case report with a favorable outcome following in utero pericardiocentesis

A. Yin, Yu-nan Wang, Chang Liu, 2021, The Journal of international medical research.

Development of a community-based hearing loss prevention and control service model in Guangdong, China

L. Du, Jieying Yang, A. Yin, 2019, BMC Public Health.

Correlation of maternal plasma total cell-free DNA and fetal DNA levels with short term outcome of first-trimester vaginal bleeding.

K. Leung, A. Yin, Yun-shao He, 2007, Human reproduction.

Prenatal genetic diagnosis of omphalocele by karyotyping, chromosomal microarray analysis and exome sequencing

Hongke Ding, Jing Wu, Jian Lu, 2021, Annals of medicine.

Analysis of amino acids and acylcarnitines profiles in small, appropriate, and large for gestational age neonates

A. Yin, S. Wen, Jinqun Liang, 2020, 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.

Prenatal chromosomal microarray analysis in foetuses with isolated absent or hypoplastic nasal bone

Jing Wu, Ling Li, Jian Lu, 2022, Annals of medicine.

Next-generation sequencing facilitates genetic diagnosis and improves the management of patients with hearing loss in clinical practice.

Fake Li, Lihua Yu, L. Du, 2021, International journal of pediatric otorhinolaryngology.

Analysis of amino acids and acyl carnitine profiles in low birth weight, preterm, and small for gestational age neonates

A. Yin, Jianhui Jiang, Jinqun Liang, 2017, 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.

Building Reproductive Genetic Services from Bottom Up: Over 30-year Experience of a Major Prenatal Diagnostic Center in Guangdong Province

A. Yin, Xiaozhuan Zhang, Jing Wu, 2013 .

Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden (HBA2:c.178G>C) and Hb Quong Sze (HBA2:c.377T>C)

L. Du, Hongke Ding, Xiuqin Bao, 2021, The Journal of international medical research.

Noninvasive detection of fetal subchromosomal abnormalities by semiconductor sequencing of maternal plasma DNA

Lianghong Zheng, Rui Hou, M. Karin, 2015, Proceedings of the National Academy of Sciences.

Performances of NIPT for copy number variations at different sequencing depths using the semiconductor sequencing platform

Dong-mei Wang, Jie-xia Yang, Yixia Wang, 2021, Human genomics.

Genetic counseling and prenatal diagnosis for hereditary hearing loss in high-risk families.

Jie-xia Yang, A. Yin, Yan Zhang, 2014, International journal of pediatric otorhinolaryngology.

Prenatal diagnosis of Miller–Dieker syndrome by chromosomal microarray

Wei He, Jing Wu, Jian Lu, 2020, Annals of human genetics.

Prenatal and perinatal outcomes of twin pregnancy discordant for one fetus with nuchal translucency above the 95th percentile

Wei He, L. Fang, Jing Wu, 2020, 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.

Reference values of fetal serum β2-microglobulin in the Chinese: evaluation of its clinical usefulness

Yanfang Zhong, D. Lu, Jing Wu, 2013, Clinical chemistry and laboratory medicine.

Characterisation of two unusual cases of haemoglobin Bart’s hydrops foetalis caused by –SEA and large novel α-globin gene cluster deletions

A. Yin, Ling Liu, L. Du, 2021, The Journal of international medical research.

Pregnancy Outcomes After Human Papillomavirus Vaccination in Periconceptional Period or During Pregnancy: A Systematic Review and Meta-analysis

M. Luo, A. Yin, Changbin Zhang, 2020, Human vaccines & immunotherapeutics.

Noninvasive Prenatal Detection of Hemoglobin Bart hydrops fetalis via maternal plasma dispensed with parental haplotyping using the Semiconductor Sequencing Platform (SSP).

L. Du, Dong-mei Wang, M. Luo, 2020, American journal of obstetrics and gynecology.

Noninvasive Prenatal Detection of Hemoglobin Bart Hydrops Fetalis Via Maternal Plasma Dispensed With Parental Haplotyping Using the Semiconductor Sequencing Platform

Dong-mei Wang, M. Luo, Jie-xia Yang, 2020 .

Genetic testing for Prader-Willi syndrome and Angelman syndrome in the clinical practice of Guangdong Province, China

L. Du, Jieying Yang, A. Yin, 2019, Molecular Cytogenetics.

Genetic counseling and prenatal diagnosis for hereditary hearing loss in high-risk families.

A. Yin, Yan Zhang, Hongke Ding, 2014, International journal of pediatric otorhinolaryngology.