Jian Li

C. Liao, Dongzhi Li, F. Fu, 2022, 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.

Antenatal screening and fetal diagnosis of β-thalassemia in a Chinese population: prevalence of the β-thalassemia trait in the Guangzhou area of China

C. Liao, Jian Li, X. Xu, 1996, Human Genetics.

Efficacy and safety of cordocentesis for prenatal diagnosis

C. Liao, Dongzhi Li, Jian Li, 2006, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

The Frequency of α-Globin Gene Triplication in a Southern Chinese Population

Dongzhi Li, Jian Li, Jian-ying Zhou, 2016, Indian Journal of Hematology and Blood Transfusion.

Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern China

C. Liao, Dongzhi Li, Jian Li, 2019, BMC Medical Genetics.

A New δ-Globin Gene Variant: Hb A2-Fengshun [δ121(GH4)Glu→Lys (HBD: c.364G > A)]

Dongzhi Li, Jian Li, Xing-mei Xie, 2016, Hemoglobin.

Phenotypic Variability in a Chinese Family with Nondeletional Hb H-Hb Quong Sze Disease

C. Liao, Dongzhi Li, Ru Li, 2011, Hemoglobin.

Prenatal diagnosis of beta-thalassemia in Southern China.

C. Liao, Dongzhi Li, Jian Li, 2006, European journal of obstetrics, gynecology, and reproductive biology.

A novel amber mutation in a β°‐thalassaemia gene (β37TGG→TAG), with direct detection by mapping the restriction fragments in amplified genomic DNA

Xiang-min Xu, C. Liao, Jian Li, 1995 .

Carrier screening for α‐ and β‐thalassemia in pregnancy: the results of an 11‐year prospective program in Guangzhou Maternal and Neonatal hospital

Xiang-min Xu, C. Liao, Jian Li, 2005 .

A novel β-globin gene deletion (codons 89–93) in a Chinese family

C. Liao, Dongzhi Li, Ru Li, 2010, Annals of Hematology.

First detection of the codons 41–43 (−CTTTG,+A) β-thalassemia mutation in a Chinese patient

C. Liao, Dongzhi Li, Jian Li, 2008, Annals of Hematology.

Detection of rare thalassemia mutations using long-read single-molecule real-time sequencing.

Feng Liu, Dongzhi Li, J. Wan, 2022, Gene.

Pregnancy outcome of autosomal aneuploidies other than common trisomies detected by noninvasive prenatal testing in routine clinical practice

C. Liao, Dongzhi Li, Ru Li, 2018, Prenatal diagnosis.

Loss-of-function variation in the DPP6 gene is associated with autosomal dominant microcephaly and mental retardation.

C. Liao, Dongzhi Li, F. Fu, 2013, European journal of medical genetics.

Carrier screening for alpha- and beta-thalassemia in pregnancy: the results of an 11-year prospective program in Guangzhou Maternal and Neonatal hospital.

Xiang-min Xu, C. Liao, Jian Li, 2005, Prenatal diagnosis.

Consequences of Delayed Prenatal Diagnosis of β-Thalassemia in Mainland China

Dongzhi Li, Ru Li, Jian Li, 2016, Hemoglobin.

Prenatal diagnosis of β-thalassemia in Southern China

C. Liao, Dongzhi Li, Jian Li, 2006 .

Diagnostic Dilemma of Hb Perth [β32(B14)Leu→Pro; HBB: c.98T > C] in Mainland China

Dongzhi Li, Jian Li, Hua Jiang, 2016, Hemoglobin.

Dominantly Inherited β-Thalassemia Caused by a Single Nucleotide Deletion in Exon 3 of the β-Globin Gene: Hb Xiangyang (HBB: c.393delT)

Dongzhi Li, Jian Li, F. Jiang, 2022, Hemoglobin.

Congenital Nonspherocytic Hemolytic Anemia Caused by Krüppel-Like Factor 1 Gene Variants: Another Case Report

Dongzhi Li, Jian Li, Hua Jiang, 2019, Hemoglobin.

KFL1 Gene Variants in α-Thalassemia Individuals with Increased Fetal Hemoglobin in a Chinese Population

C. Liao, Dongzhi Li, Jian Li, 2018, Hemoglobin.

A novel splicing mutation of ARHGAP29 is associated with nonsyndromic cleft lip with or without cleft palate

Shaoqing Wu, C. Liao, Dongzhi Li, 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.

Nonimmune Hydrops Fetalis Diagnosed during the Second Half of Pregnancy in Southern China

C. Liao, Dongzhi Li, Jian Li, 2007, Fetal Diagnosis and Therapy.

A Severe Case of Hemoglobin H Disease due to Compound Heterozygosity for Deletion of the Major α-Globin Regulatory Element (MCS-R2) and α0-Thalassemia

Dongzhi Li, Lv-Yin Huang, Jian Li, 2017, Acta Haematologica.

Hb Lepore-Hong Kong: First Report of a Novel δ/β-Globin Gene Fusion in a Chinese Family

Dongzhi Li, Jian Li, Jian-ying Zhou, 2021, Hemoglobin.

Implementation of Newborn Screening for Hemoglobin H Disease in Mainland China

C. Liao, Dongzhi Li, Ru Li, 2015, Indian Journal of Hematology and Blood Transfusion.

The detection of aneuploidy and maternal contamination by QF-PCR in samples undergoing prenatal diagnosis for thalassemia in Southern China.

C. Liao, Dongzhi Li, Xin Yang, 2009, European journal of obstetrics, gynecology, and reproductive biology.

Identification of Nondeletional α-Thalassemia in a Prenatal Screening Program by Reverse Dot-Blot in Southern China

Dongzhi Li, Ru Li, Jian Li, 2015, Hemoglobin.

Prenatal Control of Hb Bart's Disease in Southern China

C. Liao, Dongzhi Li, Jian Li, 2007, Hemoglobin.

Prenatal diagnosis of hemoglobin Bart's disease caused by co‐inheritance of two different α0‐thalassemia defects in China

C. Liao, Dongzhi Li, Jian Li, 2009, Prenatal diagnosis.

Mild hemoglobin H-constant spring disease with β-thalassemia—a case report

C. Liao, Dongzhi Li, Jian Li, 2010, Annals of Hematology.

Detection of alpha-thalassemia in beta-thalassemia carriers and prevention of Hb Bart's hydrops fetalis through prenatal screening.

C. Liao, Dongzhi Li, Jian Li, 2006, Haematologica.

Limb Defects in a Fetus with Homozygous α-Thalassemia

Dongzhi Li, Jian Li, 2008, Hemoglobin.

SHORT COMMUNICATION LIMB DEFECTS IN A FETUS WITH HOMOZYGOUS a-THALASSEMIA

Dongzhi Li, Jian Li, D. Li, 2008 .

Detection of an α-Globin Fusion Gene Using Real-Time Polymerase Chain Reaction-Based Multicolor Melting Curve

Dongzhi Li, Jian Li, F. Jiang, 2020, Hemoglobin.

Four Cases of Hb Q-H Disease Found in Southern China

C. Liao, Dongzhi Li, Jian Li, 2007, Hemoglobin.

Detection of Hb Constant Spring by a Capillary Electrophoresis Method

C. Liao, Dongzhi Li, Ru Li, 2010, Hemoglobin.

Fetal Pyruvate Kinase Deficiency Identified Incidentally in a Chinese Family at Risk for α-Thalassemia

Dongzhi Li, Jian Li, Jin Han, 2021, Indian Journal of Hematology and Blood Transfusion.

First prenatal case of 48,XXYY syndrome detected by maternal cell-free DNA testing

Dongzhi Li, L. Zhen, M. Pan, 2020, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.

Three Hemoglobin Variants Caused by a Single α-Chain Gene Mutation in a Chinese Family

C. Liao, Dongzhi Li, Jian Li, 2009, Acta Haematologica.

Regulatory Single Nucleotide Polymorphism rs368698783 (G>A): a Genetic Modifier of Hb F Production Only under Erythropoietic Stress Characteristic for β-Globin Chain Deficiency?

C. Liao, Dongzhi Li, Jian Li, 2019, Hemoglobin.

A Double Heterozygote for (δβ)0-Thalassemia and Codons 41/42 (–TTCT) Behaves as a Homozygote for the Frameshift Mutation in a Chinese Family

C. Liao, Dongzhi Li, Jian Li, 2007, Hemoglobin.

Hydrops Fetalis Caused by Homozygous Alpha-Thalassemia and Kidd Antigen Alloimmunization in a Chinese Woman

C. Liao, Dongzhi Li, Jian Li, 2008, Fetal Diagnosis and Therapy.

Utilization of multiple genetic methods for prenatal diagnosis of rare thalassemia variants

C. Liao, Jian Li, Fa-tao Li, 2023, Frontiers in genetics.

A novel SPTB frameshift deletion causing hereditary spherocytosis identified by next‐generation sequencing in a Chinese family

Dongzhi Li, Jian Li, Fa-tao Li, 2021, International journal of laboratory hematology.

Whole exome sequencing as a diagnostic adjunct to clinical testing in fetuses with structural abnormalities

C. Liao, Dongzhi Li, T. Lei, 2017, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Detection of fetal copy number variants by non‐invasive prenatal testing for common aneuploidies

C. Liao, Dongzhi Li, F. Fu, 2016, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Ndufa4 Regulates the Proliferation and Apoptosis of Neurons via miR-145a-5p/Homer1/Ccnd2

C. Liao, Dongzhi Li, T. Lei, 2023, Molecular Neurobiology.

[Dandy-walker syndrome and microdeletions on chromosome 7].

C. Liao, Dongzhi Li, F. Fu, 2012, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Hematological Characteristics of Hb Constant Spring (HBA2: c.427T>C) Carriers in Mainland China

Dongzhi Li, Jian Li, F. Jiang, 2020, Hemoglobin.

Misdiagnosis of Hb Constant Spring (α142, Term→Gln, TAA→CAA in α2) in a Hb H (β4) Disease Child

C. Liao, Dongzhi Li, Jian Li, 2007 .

Misdiagnosis of Hb constant spring (alpha142, Term-->Gln, TAA-->CAA in alpha2) in a Hb H (beta4) disease child.

C. Liao, Dongzhi Li, Jian Li, 2007, Hemoglobin.

First Case of a Compound Heterozygosity for Two Nondeletional α-Thalassemia mutations, Hb Constant Spring and Hb Quong Sze

Dongzhi Li, Jian Li, J. Yan, 2016, Hemoglobin.

Diversity in clinical presentation of hemoglobin H disease induced by the SEA deletion and the hemoglobin Quong Sze

C. Liao, Dongzhi Li, Jian Li, 2009, Annals of Hematology.

A β-Thalassemia Trait with Two Mutations in Cis in a Chinese Family

Dongzhi Li, L. Zhen, Jian Li, 2019, Hemoglobin.

Coinheritance of Hb City of Hope (HBB: c.208G>A) and β-Thalassemia: Compromising the Molecular Diagnosis of the Codons 71/72 (+A) (HBB: c.216_217insA) Mutation by Reverse Dot-Blot Hybridization

Dongzhi Li, Jian Li, F. Jiang, 2019, Hemoglobin.

Prenatal control of Hb Bart’s hydrops fetalis: a two-year experience at a mainland Chinese hospital

C. Liao, Dongzhi Li, Ru Li, 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.

The Codon 37 (TGG→TAG) β0-Thalassemia Mutation Found in a Chinese Family

Xue-wei Tang, C. Liao, Dongzhi Li, 2006, Hemoglobin.

First detection of the splice donor site IVS-I-2 (T-->B) beta-thalassemia mutation in a Chinese patient.

C. Liao, Dongzhi Li, Jian Li, 2005, Haematologica.

Application of real‐time PCR–based multicolor melting curve with automatic analysis system in pregestational and prenatal thalassemia diagnoses

Jian Li, F. Jiang, Xiaocheng Lin, 2023, Annals of human genetics.

C. Liao, Dongzhi Li, Jian Li, 2020, BMC Medical Genetics.

Implementation of high‐resolution SNP arrays in the investigation of fetuses with ultrasound malformations: 5 years of clinical experience

G. Xie, C. Liao, F. Fu, 2014, Clinical genetics.