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

THE CLINICAL SIGNIFICANCE OF THE SPECTRUM OF INTERACTIONS OF THE RARE IVS-II-5 G>C (HBB: C.315+5 G>C) VARIATION WITH OTHER Β-THALASSEMIA MUTATIONS IN SOUTHERN CHINA

(2022) Yali Zhou et al.   Mediterranean Journal of Hematology and Infectious Diseases

Early genetic screening uncovered a high prevalence of thalassemia among 18,309 neonates in Guizhou, China

(2021) Mei Tan et al.   CLINICAL GENETICS

A More Universal Approach to Comprehensive Analysis of Thalassemia Alleles (CATSA)

(2021) Qiaowei Liang et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Long molecule sequencing: a new approach for identification of clinically significant DNA variants in alpha and beta thalassemia carriers

(2020) Liangpu Xu et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

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

(2020) Jiachun Qin et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Next-generation sequencing improves molecular epidemiological characterization of thalassemia in Chenzhou Region, P.R. China

(2019) Haoqing Zhang et al.   JOURNAL OF CLINICAL LABORATORY ANALYSIS

Clinical Classification, Screening and Diagnosis for Thalassemia

(2018) Vip Viprakasit et al.   HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA

Next-generation sequencing improves thalassemia carrier screening among premarital adults in a high prevalence population: the Dai nationality, China

(2017) Jing He et al.   GENETICS IN MEDICINE

Simultaneous Genotyping of α-Thalassemia Deletional and Nondeletional Mutations by Real-Time PCR–Based Multicolor Melting Curve Analysis

(2017) Qiuying Huang et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Investigation of mutations in the HBB gene using the 1,000 genomes database

(2017) Tânia Carlice-dos-Reis et al.   PLoS One

Rapid detection of G6PD mutations by multicolor melting curve analysis

(2016) Zhongmin Xia et al.   MOLECULAR GENETICS AND METABOLISM

The Prevalence and Molecular Spectrum of α- and β-Globin Gene Mutations in 14,332 Families of Guangdong Province, China

(2014) Aihua Yin et al.   PLoS One

A novel fusion gene and a common α0-thalassemia deletion cause hemoglobin H disease in a Chinese family

(2013) Ji-Wei Huang et al.   BLOOD CELLS MOLECULES AND DISEASES

A Melting Curve Analysis–Based PCR Assay for One-Step Genotyping of β-Thalassemia Mutations

(2011) Fu Xiong et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Molecular epidemiological survey of haemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China

(2010) F Xiong et al.   CLINICAL GENETICS