Q. Fang

发表

Chromosomal abnormalities detected by karyotyping and microarray analysis in twins with structural anomalies

Shaobin Lin, Linhuan Huang, Xuan Huang, 2020, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Prenatal diagnosis of posterior fossa anomalies: Additional value of chromosomal microarray analysis in fetuses with cerebellar hypoplasia

Shaobin Lin, Linhuan Huang, Yanmin Luo, 2018, Prenatal diagnosis.

Placental NFE2L2 is discordantly activated in monochorionic twins with selective intrauterine growth restriction and possibly regulated by hypoxia

Guanglan Zhang, Xuan Huang, Yu Gao, 2017, Free radical research.

Discordant HIF1A mRNA levels and oxidative stress in placental shares of monochorionic twins with selective intra-uterine growth restriction.

Z. He, Zhi-ming He, Q. Fang, 2015, Placenta.

Replication timing regulation in adults with chromosomal balance rearrangements.

Y. Xie, Jian-zhu Wu, Q. Fang, 2015, Genetics and molecular research : GMR.

Application of chromosomal microarray analysis in prenatal diagnosis of fetal growth restriction

Shaobin Lin, Linhuan Huang, Yi Zhou, 2016, Prenatal Diagnosis.

Smith‑Magenis syndrome in monozygotic twin fetuses presenting with discordant phenotypes and uteroplacental insufficiency.

Yi Zhou, Jian-zhu Wu, Q. Fang, 2015, Molecular medicine reports.

Imprinting and Promoter Usage of Insulin-Like Growth Factor II in Twin Discordant Placenta

G. Zhuang, Linhuan Huang, Yanmin Luo, 2010, Obstetrics and gynecology international.

Chromosomal aberrations and CNVs in twin fetuses with cardiovascular anomalies: Comparison between monochorionic diamniotic and dichorionic diamniotic twins

Shaobin Lin, Linhuan Huang, Yanmin Luo, 2018, Prenatal diagnosis.

Placental expression of PHLDA2 in selective intrauterine growth restriction in monozygotic twins.

Yongde Luo, Q. Fang, C. Gou, 2014, Placenta.

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.

Chromosome 10q26 deletion syndrome: Two new cases and a review of the literature

Shaobin Lin, Yi Zhou, Yanmin Luo, 2016, Molecular medicine reports.

Preeclampsia in twin pregnancies: association with selective intrauterine growth restriction

Dongcai Wu, Linhuan Huang, Yanmin Luo, 2015, 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.

Improved assay performance of single nucleotide polymorphism array over conventional karyotyping in analyzing products of conception

Yi Zhou, Shaobin Lin, Shanshan Shi, 2015, Journal of the Chinese Medical Association : JCMA.

Prenatal management and outcomes in mirror syndrome associated with twin–twin transfusion syndrome

Yi Zhou, Yanmin Luo, Xuan Huang, 2014, Prenatal diagnosis.

Noninvasive Prenatal Detection for Pathogenic CNVs: The Application in α-Thalassemia

N. Chen, Hui Jiang, Fang Chen, 2013, PloS one.

Prenatal treatment of severe fetal hemolytic disease due to anti-M alloimmunization by serial intrauterine transfusions.

Linhuan Huang, Yanmin Luo, G. Luo, 2017, Taiwanese journal of obstetrics & gynecology.

Placental Expressions of CDKN1C and KCNQ1OT1 in Monozygotic Twins with Selective Intrauterine Growth Restriction

Xuan Huang, Xiangzhen Liu, Q. Fang, 2017, Twin Research and Human Genetics.

The promoter methylomes of monochorionic twin placentas reveal intrauterine growth restriction-specific variations in the methylation patterns

Junwen Wang, Huijuan Luo, Hanlin Lu, 2016, Scientific Reports.

Placental expression of osteopontin(OPN) in monochorionic twins with discordant growth.

Y. Zhou, Q. Fang, Y. Gao, 2013, Placenta.

miRNA‐210‐3p regulates trophoblast proliferation and invasiveness through fibroblast growth factor 1 in selective intrauterine growth restriction

Y. Xiong, Xuan Huang, Lin Li, 2019, Journal of cellular and molecular medicine.

Placental characteristics in monochorionic twins with selective intrauterine growth restriction assessed by gradient angiography and three-dimensional reconstruction

Yi Zhou, Xuan Huang, Xiangzhen Liu, 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.

Selective and non-selective intrauterine growth restriction in twin pregnancies: high-risk factors and perinatal outcome

Linhuan Huang, Yi Zhou, Yanmin Luo, 2012, Archives of Gynecology and Obstetrics.

Hemolytic disease of the fetus and newborn due to alloanti-M: three Chinese case reports and a review of the literature.

Linhuan Huang, G. Luo, Q. Fang, 2018, Transfusion.

Prenatal diagnosis of fetuses with Emanuel syndrome: Results of ultrasound examination and invasive genetic testing

Jian-zhu Wu, Q. Fang, Yuqing Deng, 2022, Prenatal diagnosis.

Transition of LINE-1 DNA Methylation Status and Altered Expression in First and Third Trimester Placentas

Jinping Li, Shi-Wen Jiang, Y. Hwa, 2014, PloS one.

Identification of compound heterozygous variants in the noncoding RNU4ATAC gene in a Chinese family with two successive foetuses with severe microcephaly

D. Cooper, C. Férec, Xueli Wu, 2018, Human Genomics.

Two novel mutations in the PPIB gene cause a rare pedigree of osteogenesis imperfecta type IX.

Wei Zhang, Weiying Jiang, Z. Fang, 2017, Clinica chimica acta; international journal of clinical chemistry.

Successful management of a hydropic fetus with severe anemia and thrombocytopenia caused by anti-CD36 antibody

S. Santoso, W. Xia, X. Ye, 2018, International Journal of Hematology.

Clinical and molecular cytogenetic studies of an unrecognised 22q11.2 deletion in three families

Linhuan Huang, Danlei Cai, Yi Zhou, 2015, Experimental and therapeutic medicine.

Discordant phenotypes in monozygotic twins with 16p11.2 microdeletions including the SH2B1 gene

Shaobin Lin, Linhuan Huang, Yanmin Luo, 2017, American journal of medical genetics. Part A.

Differing Microdeletion Sizes and Breakpoints in Chromosome 7q11.23 in Williams-Beuren Syndrome Detected by Chromosomal Microarray Analysis

Shaobin Lin, Linhuan Huang, Yanmin Luo, 2016, Molecular Syndromology.

22q12.3 microduplication overlapping the LARGE gene as a male-only affected loci responsible for increasing the risk of autism spectrum disorder.

Xuan Huang, Q. Fang, Yingjun Xie, 2017, Biomedical reports.

Prenatal Diagnosis and Management of Monozygotic Twins Discordant for Turner Syndrome

Yu Gao, Q. Fang, C. Gou, 2013, Fetal Diagnosis and Therapy.

Increased Expression and Altered Methylation of HERVWE1 in the Human Placentas of Smaller Fetuses from Monozygotic, Dichorionic, Discordant Twins

Linhuan Huang, Yi Zhou, Yanmin Luo, 2012, PloS one.

Mucopolysaccharidosis type IIIB mutations in Chinese patients: identification of two novel NAGLU mutations and analysis of two cases involving prenatal diagnosis.

M. Du, Weiying Jiang, Jing-xin Pan, 2013, Clinica chimica acta; international journal of clinical chemistry.

CXCR2 is decreased in preeclamptic placentas and promotes human trophoblast invasion through the Akt signaling pathway.

Dongcai Wu, Linhuan Huang, Yanmin Luo, 2016, Placenta.

Prenatal diagnosis of Sotos syndrome characterized by fetal growth restriction

Shaobin Lin, Q. Fang, Yi Zhang, 2017, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

Aberrant hydroxymethylation of ANGPTL4 is associated with selective intrauterine growth restriction in monochorionic twin pregnancies

M. Zhong, Q. Fang, Yi Zhang, 2020, Epigenetics.

Distribution of maternal red cell antibodies and the risk of severe alloimmune haemolytic disease of the foetus in a Chinese population: a cohort study on prenatal management

Yanmin Luo, Yu Gao, G. Luo, 2020, BMC Pregnancy and Childbirth.

Insulin-like growth factor binding protein 1 and human embryonic development during 6 - 10 gestational weeks.

Yi Zhou, Yan-xia Wang, Q. Fang, 2004, Chinese Medical Journal.

Study on the Imprinting Status of Insulin-Like Growth Factor II (IGF-II) Gene in Villus during 6–10 Gestational Weeks

Yi Zhou, Yanmin Luo, Q. Fang, 2010, Obstetrics and gynecology international.

[Relationship between the genotype and hematologic characteristics in the fetuses with thalassemia].

Linhuan Huang, Yi Zhou, Yanmin Luo, 2006, Zhonghua er ke za zhi = Chinese journal of pediatrics.

[Investigation of ultrasound markers in screening fetal trisomy 21].

Hongning Xie, Jian-zhu Wu, Q. Fang, 2013, Zhonghua fu chan ke za zhi.