周万军｜南方医科大学｜学者主页

2026

Detection of Allergy-Related TPSAB1 Copy Number Variation by MALDI-TOF Nucleic Acid Mass Spectrometry.

Yang Li, Xue-Feng Zhao, Sheng He, Yun-Li Lai, Shijie Wei, Wanjun Zhou

Clinical Laboratory

DOI

2026

Simultaneous detection of SMN1, SMN2, NAIP, H4F5, GTF2H2 copy number and SMN1 loss-of-function variants for SMA by MALDI-TOF mass spectrometry.

Yun-Li Lai, Ya-Jun Cheng, Xuexi Yang, Biyan Cheng, Rui Zhong, Shijie Wei, Ting Que, Sheng He, Wanjun Zhou

Journal of Molecular Diagnostics

DOI

2025

单分子实时测序在α珠蛋白基因三联体及其复合变异等位基因鉴定中的临床应用

张宇，方艳平，朱碧青，梁丽仪，周万军，江凌晓

《国际检验医学杂志》

2025

A multiplex allele specific PCR capillary electrophoresis (mASPCR-CE) assay for simultaneously analysis of SMN1/SMN2/NAIP copy number and SMN1 loss-of-function variants

Yun-Li Lai, Xu Yang, Shijie Wei, Yajun Chen, Yanjun Cai, Wenyu Wang, Zeyan Zhong, Xue-Xi Yang, Wanjun Zhou

Clinical Chemistry and Laboratory Medicine

DOI

2025

Screening G6PD mutation in blood donors by Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry with high-throughput and multiple targets.

Zi-Yan Li, Zhenyi Huang, Meng-Xia Li, Yunshan Cao, Yating Li, Jinlv Liu, Suping Zhong, Li-Juan Lin, Yan-Ping Fang, Zhaoying Su, Yong-Xin Huang, Wanjun Zhou, Ling-Xiao Jiang

Journal of Molecular Diagnostics

DOI

2024

Information needs preferences of Chinese colorectal cancer patients receiving chemotherapy: A discrete choice experiment

Linlin Li, Xueli Liu, Wanjun Zhou, Yawen Zhang, Xinqiong Zhang

Asia-Pacific Journal Of Oncology Nursing，Vol. 11, No. 90

DOI

2024

Prevalence of thalassaemia among childbearing-age Li and Han populations in Hainan Province

Fangchao Tao, Yan-Quan Lai, Jiaqi Chen, Shijie Wei, Y. Zou, Yun-Li Lai, Qiongzhen Qin, Yufeng Wang, Wanjun Zhou

Hematology

DOI

2024

SNPscan Combined With CNVplex as a High‐Performance Diagnostic Method for Thalassemia

Xiao-Feng Wei, Xingmin Wang, Fu Xiong, Xinhua Zhang, Dun Liu, Wanjun Zhou, F. He, Xuan Shang

Prenatal Diagnosis

DOI

2023

佛山地区55例新生儿血红蛋白E合并地中海贫血病例的基因型和血液型特征分析

林粤，周万军，余丰，张澎怡，刘海平，余楠

《分子诊断与治疗杂志》

2023

Nanopore Third-Generation Sequencing for Comprehensive Analysis of Hemoglobinopathy Variants

Weilun Huang, Shoufang Qu, Qiongzhen Qin, Xu Yang, Xu Yang, Wanqing Han, Yongli Lai, Jiaqi Chen, Shihao Zhou, Xuexi Yang, Xuexi Yang, Wanjun Zhou

Clinical Chemistry

DOI

2023

Target-allele-specific probe single-base extension (TASP-SBE): a novel MALDI–TOF–MS strategy for multi-variants analysis and its application in simultaneous detection of α-/β-thalassemia mutations

Qiong Chen, Xuexi Yang, Weilun Huang, Ziyan Li, Mingli Xu, Yang Li, Fangchao Tao, Zhengyi Huang, Xu Yang, Xüe-Feng Zhao, Linxiao Jiang, Wanjun Zhou

Human Genetics

DOI

2022

红细胞渗透脆性试验参考区间的建立及在地中海贫血筛查中的初步应用

何思华，方艳平，林丽娟，李紫岩，黄振艺，周万军，江凌晓

《热带医学杂志》

2022

One-step genotyping of α-thalassaemia by multiplex symmetric PCR melting curve

Jiachun Qin, Jun He, Yang Li, Nansong Liu, Fangchao Tao, Pengyi Zhang, Weilin Guo, Qiongzhen Qin, Wanjun Zhou

Journal of Clinical Pathology

DOI

2022

Molecular spectrum of thalassemia in tropical Hainan Island of southern China: high allele frequency with low health burden

Yanquan Lai, Fangchao Tao, Yu Feng Zou, Min Huang, Kaiting Lin, Yang Li, Weilun Huang, Wanjun Zhou

Journal of genetics and genomics/Journal of Genetics and Genomics

DOI

2021

希特林蛋白缺乏症实时荧光PCR解链曲线快速基因分型的建立与应用

刘海平，秦佳纯，袁伟曦，黄伟伦，周万军

《临床检验杂志》

DOI

2020

地中海贫血分子诊断技术进展

贺骏，秦佳纯，周万军

《中国临床新医学》

2020

Characterization of a Novel 71.8 kb α0-Thalassemia Deletion and Subsequent Summary of a Practical Procedure for Thalassemia Molecular Diagnosis

Mingli Xu, Jiachun Qin, Bi-Yan Chen, Xuexi Yang, Haiping Liu, Weixi Yuan, Jianmei Zhong, Limin Huang, Wanjun Zhou

Hemoglobin

DOI

2020

A Nested Asymmetric PCR Melting Curve Assay for One-Step Genotyping of Nondeletional α-Thalassemia Mutations

Jiachun Qin, Mingli Xu, Qiang Zhang, Xiaojun Wen, sheng tao he, Yong Zhou, Haiping Liu, Wanjun Zhou

Journal of Molecular Diagnostics

DOI

2020

Characterization of two novel Alu element-mediated α-globin gene cluster deletions causing α0-thalassemia by targeted next-generation sequencing

Zhiming Li, Xuan Shang, Shiqiang Luo, Fei Zhu, Xiaofeng Wei, Wanjun Zhou, Yuhua Ye, Tizhen Yan, Ren Cai, Xiangmin Xu

Molecular Genetics and Genomics

DOI

2019

Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease

Shun-Chang Sun, Di Ma, Meiyi Li, Ruxu Zhang, Cheng Huang, Huajie Huang, Yongzhi Xie, Zhong-Ju Wang, Jun Liu, Decheng Cai, Cuixian Liu, Qi Yang, Feixiang Bao, Xiaoli Gong, Jie-Ru Li, Hui Zheng, Xiaofeng Wei, Jianmei Zhong, Wanjun Zhou, Xuan Shang, Cheng Zhang, Xingguo Liu, Beisha Tang, Fu Xiong, Xiang-Min Xu

Brain

DOI

2019

A Cell‐free DNA Barcode‐Enabled Single‐Molecule Test for Noninvasive Prenatal Diagnosis of Monogenic Disorders: Application to β‐Thalassemia

Xingkun Yang, Qinghua Zhou, Wanjun Zhou, Mei Zhong, Xiaoling Guo, Xiaofeng Wang, Xin Fan, Shanhuo Yan, Liyan Li, Yunli Lai, Yongli Wang, Jin Huang, Yuhua Ye, Huaping Zeng, Jun Chuan, Yuanping Du, Chouxian Ma, Peining Li, Zhuo Song, Xiangmin Xu

Advanced Science

DOI

2018

囊胚细胞WGA结合短片段Gap-PCR的α-地贫SEA突变快速植入前遗传学诊断

徐惠玲，刘彦慧，晏平，何怡，秦佳纯，娄季武，周万军

《南方医科大学学报》

2018

[Non-invasive prenatal diagnosis for beta-thalassemia by detecting paternal CD41-42 mutation in cell-free DNA derived from maternal plasma with droplet digital PCR].

Zhang Yijia, Xiao-Qian Gong, Yi He, Lichan Huang, Qiang Zhang, Yanhui Liu, Jiufeng Li, Yajun Chen, Wanjun Zhou

PubMed

DOI

2018

[Genetic and phenotypic analysis of a rare case with homozygous Chinese Gγ (Aγδβ)0-thal deletion].

Qiang Zhang, Yijia Zhang, Huiling Xu, Mingli Xu, Xiaojun Wen, Xiangmin Xu, Wanjun Zhou

PubMed

DOI

2018

Systematic assessment of the performance of whole-genome amplification for SNP/CNV detection and β-thalassemia genotyping

Fei He, Wanjun Zhou, Ren Cai, Tizhen Yan, Xiangmin Xu

Journal of Human Genetics

DOI

2018

[Rapid preimplantation genetic diagnosis of α-thalassemia SEA deletion with blastocyst cell whole genome amplification and short fragment Gap-PCR method].

Huiling Xu, Yanhui Liu, Ping Yan, Yi He, Jiachun Qin, Jiwu Lou, Wan-Jun Zhou

PubMed

DOI

2017

微滴式数字PCR（ddPCR）快速检测α珠蛋白基因αααanti-3.7三联体

龚小倩，杨学煌，乔伶俐，陈亚军，周万军

《南方医科大学学报》

2017

Rapid Targeted Next-Generation Sequencing Platform for Molecular Screening and Clinical Genotyping in Subjects with Hemoglobinopathies

Xuan Shang, Zhiyu Peng, Yuhua Ye, Asan, Xinhua Zhang, Yan Chen, Baosheng Zhu, Wangwei Cai, Shaoke Chen, Ren Cai, Xiaoling Guo, Chonglin Zhang, Yuqiu Zhou, Shuodan Huang, Yanhui Liu, Biyan Chen, Shanhuo Yan, Yajun Chen, Hongmei Ding, Xiaolin Yin, Liu-Song Wu, Jing He, Dehao Huang, sheng tao he, Tizhen Yan, Xin Fan, Yuehong Zhou, Xiaofeng Wei, Sumin Zhao, Decheng Cai, Fengyu Guo, Qianqian Zhang, Yun Li, Xuelian Zhang, Haorong Lu, Huajie Huang, Junfu Guo, Fei Zhu, Yuan Yuan, Li Zhang, Na Liu, Zhiming Li, Hui Jiang, Qiang Zhang, Yijia Zhang, Wan Khairunnisa Wan Juhari, Sarifah Hanafi, Wanjun Zhou, Fu Xiong, Huanming Yang, jian Zi Wang, Bin Alwi Zilfalil, Ming Qi, Yaping Yang, Ye Yin, Mao Mao, Xiangmin Xu

EBioMedicine

DOI

2017

Hb H Disease Caused by Multiple Mutations in the Polyadenylation Signal Site and − −SEA/αα

Zhang Qiang, Xin Fan, Mingli Xu, Yijia Zhang, Huiling Xu, Xiaojun Wen, Wanjun Zhou

Hemoglobin

DOI

2017

α+-Thalassemia Caused by an 811 bp Deletion in Individuals from Nanning, Guangxi: A Report of Two Cases

Qiang Zhang, Mingli Xu, Wanjun Zhou, Xin Fan

Hemoglobin

DOI

2016

一种罕见α-地贫基因突变HbH病(--SEA/α*92A>Gα)的家系分析与基因诊断

颜善活，劳可干，符可鹏，龚菲菲，温晓君，周万军

《南方医科大学学报》

2016

高分辨率熔解曲线法检测药物性耳聋相关线粒体12S rRNA突变

温晓君，颜善活，胡伟群，周万军

《临床检验杂志》

DOI

2016

Evaluation and comparison of three assays for molecular detection of spinal muscular atrophy

Li Liang, Wanjun Zhou, Ping Fang, Zeyan Zhong, Jiansheng Xie, Tizhen Yan, Jian Zeng, Xu-Hui Tan, Xiangmin Xu

Clinical Chemistry and Laboratory Medicine (CCLM)

DOI

2016

A splicing mutation in VPS4B causes dentin dysplasia I

Qi Yang, Dong Chen, Fu Xiong, Danna Chen, Cuixian Liu, Yanhui Liu, Qiuxia Yu, Jun Xiong, Jinzhong Liu, Kunyang Li, Lingfeng Zhao, Yuhua Ye, Hong Wei Zhou, Lingling Hu, Zhihui Tian, Xuan Shang, Leitao Zhang, Xiaofeng Wei, Wanjun Zhou, Dong‐Ri Li, Wenqing Zhang, Xiangmin Xu

Journal of Medical Genetics

DOI

2015

加尾引物多重PCR技术检测Y染色体微缺失

邹德亮，温晓君，张雪莲，吴晓伟，周万军，吴英松

《陆军军医大学学报》

2015

Human STEAP3 mutations with no phenotypic red cell changes

Dun Liu, Sheng Yi, Xinhua Zhang, Xinhua Zhang, Ping Fang, Chenguang Zheng, Li Lin, Ren Cai, Yuhua Ye, Yuqiu Zhou, Yunhao Liang, Feng Cheng, Xuelian Zhang, Xuelian Zhang, Wanjun Zhou, Narla Mohandas, Xiuli An, Xiangmin Xu

Blood

DOI

2015

First Description of aβ-Thalassemia Mutation, −86 (C > G) (HBB: c.−136C > G), in a Chinese Family

sheng tao he, Qian Qin, Shang Yi, Wanjun Zhou, Jianping Deng, Chenguang Zheng, Biyan Chen

Hemoglobin

DOI

2015

Development of a capillary zone electrophoresis method for rapid determination of human globin chains in α and β-thalassemia subjects

Li Lin, Danna Chen, Jing Guo, Wanjun Zhou, Xiangmin Xu

Blood Cells Molecules and Diseases

DOI

2015

Molecular characterization and copy number of SMN1, SMN2 and NAIP in Chinese patients with spinal muscular atrophy and unrelated healthy controls

Ping Fang, Liang Li, Jian Zeng, Wanjun Zhou, Weiqing Wu, Zeyan Zhong, Tizhen Yan, Jiansheng Xie, Jing Huang, Lin Li, Ying Xin Zhao, Xiangmin Xu

BMC Musculoskeletal Disorders

DOI

2014

四重TaqMan实时荧光PCR检测α地中海贫血——SEA、—α3.7和—α4.2缺失

赵学峰，王格，周万军

《临床检验杂志》

2014

α和β地中海贫血无创产前诊断研究进展

周万军，徐湘民

《国际生殖健康/计划生育杂志》

2014

基因拷贝数定量检测在缺失型α-地贫快速诊断中的应用

胥顺，周万军，牟毅，程钢

《分子诊断与治疗杂志》

2013

A Multiplex qPCR Gene Dosage Assay for Rapid Genotyping and Large-Scale Population Screening for Deletional α-Thalassemia

Wanjun Zhou, Ge Wang, Xue-feng Zhao, Fu Xiong, Shaoxiong Zhou, Jianming Peng, Youming Cheng, Shun Xu, Xiangmin Xu

Journal of Molecular Diagnostics

DOI

2012

基于父源差异SNP位点的等位基因特异性实时荧光PCR方法建立及其在α0-地中海贫血无创产前诊断中的应用

刘彦慧，吴亚敏，石少权，娄季武，马秋林，何怡，徐婉芳，林洋洋，周万军

《陆军军医大学学报》

2012

Rapid simultaneous genotyping of polymorphisms in ADH1B and ALDH2 using high resolution melting assay

Xiao-Wen Yuan, Wanjun Zhou, Xuan Shang, Liang Li, Yan‐Hui Liu, Xiangmin Xu

Clinical Chemistry and Laboratory Medicine (CCLM)

DOI

2012

Analyses of GATA4, NKX2.5, and TFAP2B genes in subjects from southern China with sporadic congenital heart disease

Fu Xiong, Qian Li, Cuimei Zhang, Youming Chen, Ping Li, Xiaofeng Wei, Qiang Li, Wanjun Zhou, Liang Li, Xuan Shang, Xiangmin Xu

Cardiovascular Pathology

DOI

2012

Rapid determination of human globin chains using reversed-phase high-performance liquid chromatography

Junhui Wan, Pei-Ling Tian, Weihao Luo, Bingyi Wu, Fu Xiong, Wanjun Zhou, Xiangcai Wei, Xiangmin Xu

Journal of Chromatography B

DOI

2012

A quantitative assay to detect α-thalassemia deletions and triplications using multiplex nested real-time quantitative polymerase chain reaction

Wanjun Zhou, Wei-Yu Liu, Dun Liu, Jian‐Hui Jiang, Dian-Min Zhou, Zeyan Zhong, Xiangmin Xu

Analytical Biochemistry

DOI

2011

开办“地中海贫血技术骨干培训班”的教学实践

李亮，周万军，熊符，商璇，魏小凤

《继续医学教育》

2011

用基因拷贝数直接定量快速诊断缺失型α地贫及人ξ珠蛋白ELISA定量检测方法的建立与应用

周万军

《南方医科大学》

2011

Reliable Detection of Paternal SNPs within Deletion Breakpoints for Non-Invasive Prenatal Exclusion of Homozygous α0-Thalassemia in Maternal Plasma

Tizhen Yan, Qiuhua Mo, Ren Cai, Xue Chen, Cui-Mei Zhang, Yan‐Hui Liu, Yajun Chen, Wanjun Zhou, Fu Xiong, Xiangmin Xu

PLoS ONE

DOI

2011

The establishment and application of double TaqMan real-time fluorescence nested PCR method for rapid detection of α-thalassemia SEA deletion

Xiao-Wen Yuan, Qian Huang, Wanjun Zhou

Zhonghua jianyan yixue zazhi

DOI

2011

Rapid, accurate detection of TMPRSS6 gene causative mutations with a high-resolution melting assay

Heming Wu, Liang Li, Xiao-Wen Yuan, Yu-Qiu Zhou, Qizhi Xiao, Wei-Yu Liu, Wanjun Zhou, Xiangmin Xu

Blood Cells Molecules and Diseases

DOI

2010

三重实时荧光PCR相对定量法快速诊断21和X染色体数目异常

刘彦慧，吴亚敏，黎丽芬，李超强，周万军

《陆军军医大学学报》

2010

Creative teaching model of medical genetics

Wanjun Zhou, Yang Hai-ying, Xiangmin Xu

Chinese Journal of Medical Education

DOI

2009

医学遗传学课堂教学与临床应用相结合的教学探讨

熊符，商璇，李莉艳，李亮，周万军

《基础医学教育》

2008

[A community-based genetic screening of large-scale population and prenatal diagnosis for alpha and beta thalassemia in Zhuhai city of Guangdong province].

Yu-qiu Zhou, Qiuhua Mo, Jin-han Lu, Liyan Li, Xiong Liang, Shiqi Jia, Ge-fei Xiao, Wanjun Zhou, Qizhi Xiao, Xiangmin Xu

PubMed

2008

Rapid genotyping of known mutations and polymorphisms in β-globin gene based on the DHPLC profile patterns of homoduplexes and heteroduplexes

Qiang Li, Liyan Li, Sheng‐Wen Huang, Liang Li, Xiaowei Chen, Wanjun Zhou, Xiangmin Xu

Clinical Biochemistry

DOI

2008

[Identification of a missense mutation in SEDL gene from a Chinese family with X-linked spondyloepiphyseal dysplasia tarda].

Wanjun Zhou, Shi-yuan Zhou, Sheng‐Wen Huang, Jiping Zhou, Xiangmin Xu

PubMed

精选作品

期刊论文

Detection of Allergy-Related TPSAB1 Copy Number Variation by MALDI-TOF Nucleic Acid Mass Spectrometry.

Simultaneous detection of SMN1, SMN2, NAIP, H4F5, GTF2H2 copy number and SMN1 loss-of-function variants for SMA by MALDI-TOF mass spectrometry.

单分子实时测序在α珠蛋白基因三联体及其复合变异等位基因鉴定中的临床应用

A multiplex allele specific PCR capillary electrophoresis (mASPCR-CE) assay for simultaneously analysis of SMN1/SMN2/NAIP copy number and SMN1 loss-of-function variants

Screening G6PD mutation in blood donors by Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry with high-throughput and multiple targets.

Information needs preferences of Chinese colorectal cancer patients receiving chemotherapy: A discrete choice experiment

Prevalence of thalassaemia among childbearing-age Li and Han populations in Hainan Province

SNPscan Combined With CNVplex as a High‐Performance Diagnostic Method for Thalassemia

佛山地区55例新生儿血红蛋白E合并地中海贫血病例的基因型和血液型特征分析

Nanopore Third-Generation Sequencing for Comprehensive Analysis of Hemoglobinopathy Variants

Target-allele-specific probe single-base extension (TASP-SBE): a novel MALDI–TOF–MS strategy for multi-variants analysis and its application in simultaneous detection of α-/β-thalassemia mutations

红细胞渗透脆性试验参考区间的建立及在地中海贫血筛查中的初步应用

One-step genotyping of α-thalassaemia by multiplex symmetric PCR melting curve

Molecular spectrum of thalassemia in tropical Hainan Island of southern China: high allele frequency with low health burden

希特林蛋白缺乏症实时荧光PCR解链曲线快速基因分型的建立与应用

地中海贫血分子诊断技术进展

Characterization of a Novel 71.8 kb α0-Thalassemia Deletion and Subsequent Summary of a Practical Procedure for Thalassemia Molecular Diagnosis

A Nested Asymmetric PCR Melting Curve Assay for One-Step Genotyping of Nondeletional α-Thalassemia Mutations

Characterization of two novel Alu element-mediated α-globin gene cluster deletions causing α0-thalassemia by targeted next-generation sequencing

Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease

A Cell‐free DNA Barcode‐Enabled Single‐Molecule Test for Noninvasive Prenatal Diagnosis of Monogenic Disorders: Application to β‐Thalassemia

囊胚细胞WGA结合短片段Gap-PCR的α-地贫SEA突变快速植入前遗传学诊断

[Non-invasive prenatal diagnosis for beta-thalassemia by detecting paternal CD41-42 mutation in cell-free DNA derived from maternal plasma with droplet digital PCR].

[Genetic and phenotypic analysis of a rare case with homozygous Chinese Gγ (Aγδβ)0-thal deletion].

Systematic assessment of the performance of whole-genome amplification for SNP/CNV detection and β-thalassemia genotyping

[Rapid preimplantation genetic diagnosis of α-thalassemia SEA deletion with blastocyst cell whole genome amplification and short fragment Gap-PCR method].

微滴式数字PCR（ddPCR）快速检测α珠蛋白基因αααanti-3.7三联体

Rapid Targeted Next-Generation Sequencing Platform for Molecular Screening and Clinical Genotyping in Subjects with Hemoglobinopathies

Hb H Disease Caused by Multiple Mutations in the Polyadenylation Signal Site and − −SEA/αα

α+-Thalassemia Caused by an 811 bp Deletion in Individuals from Nanning, Guangxi: A Report of Two Cases

一种罕见α-地贫基因突变HbH病(--SEA/α*92A>Gα)的家系分析与基因诊断

高分辨率熔解曲线法检测药物性耳聋相关线粒体12S rRNA突变

Evaluation and comparison of three assays for molecular detection of spinal muscular atrophy

A splicing mutation in VPS4B causes dentin dysplasia I

加尾引物多重PCR技术检测Y染色体微缺失

Human STEAP3 mutations with no phenotypic red cell changes

First Description of aβ-Thalassemia Mutation, −86 (C > G) (HBB: c.−136C > G), in a Chinese Family

Development of a capillary zone electrophoresis method for rapid determination of human globin chains in α and β-thalassemia subjects

Molecular characterization and copy number of SMN1, SMN2 and NAIP in Chinese patients with spinal muscular atrophy and unrelated healthy controls

四重TaqMan实时荧光PCR检测α地中海贫血——SEA、—α3.7和—α4.2缺失

α和β地中海贫血无创产前诊断研究进展

基因拷贝数定量检测在缺失型α-地贫快速诊断中的应用

A Multiplex qPCR Gene Dosage Assay for Rapid Genotyping and Large-Scale Population Screening for Deletional α-Thalassemia

基于父源差异SNP位点的等位基因特异性实时荧光PCR方法建立及其在α0-地中海贫血无创产前诊断中的应用

Rapid simultaneous genotyping of polymorphisms in ADH1B and ALDH2 using high resolution melting assay

Analyses of GATA4, NKX2.5, and TFAP2B genes in subjects from southern China with sporadic congenital heart disease

Rapid determination of human globin chains using reversed-phase high-performance liquid chromatography

A quantitative assay to detect α-thalassemia deletions and triplications using multiplex nested real-time quantitative polymerase chain reaction

开办“地中海贫血技术骨干培训班”的教学实践

用基因拷贝数直接定量快速诊断缺失型α地贫及人ξ珠蛋白ELISA定量检测方法的建立与应用

Reliable Detection of Paternal SNPs within Deletion Breakpoints for Non-Invasive Prenatal Exclusion of Homozygous α0-Thalassemia in Maternal Plasma

The establishment and application of double TaqMan real-time fluorescence nested PCR method for rapid detection of α-thalassemia SEA deletion

Rapid, accurate detection of TMPRSS6 gene causative mutations with a high-resolution melting assay

三重实时荧光PCR相对定量法快速诊断21和X染色体数目异常

Creative teaching model of medical genetics

医学遗传学课堂教学与临床应用相结合的教学探讨

[A community-based genetic screening of large-scale population and prenatal diagnosis for alpha and beta thalassemia in Zhuhai city of Guangdong province].

Rapid genotyping of known mutations and polymorphisms in β-globin gene based on the DHPLC profile patterns of homoduplexes and heteroduplexes

[Identification of a missense mutation in SEDL gene from a Chinese family with X-linked spondyloepiphyseal dysplasia tarda].

会议论文

毛细管区带电泳法快速分离珠蛋白肽链及其应用研究

Multiple STEAP3 loss-of-function heterozygous mutations identified in the Chinese population with no phenotypic red cell alterations

1998—2010年珠海市地中海贫血大规模人群的遗传筛查和产前诊断结果分析

珠蛋白基因拷贝数相对定量快速检测α-地贫-SEA、-α3.7和-α4.2缺失方法的建立与应用

反相高效液相色谱快速分离珠蛋白肽链及其应用研究

用基因拷贝数直接定量快速诊断缺失型α地贫

研究方向