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

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

Molecular Basis and Genetic Modifiers of Thalassemia

(2018) Sachith Mettananda et al.   HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA

Prenatal and preimplantation diagnosis of hemoglobinopathies

(2018) C. Vrettou et al.   International Journal of Laboratory Hematology

Thalassaemia

(2018) Ali T Taher et al.   LANCET

Preconception carrier screening and prenatal diagnosis in thalassemia and hemoglobinopathies: challenges and future perspectives

(2017) Joanne Traeger-Synodinos et al.   EXPERT REVIEW OF MOLECULAR DIAGNOSTICS

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

Design, Validation, and Clinical Implementation of a Gap-Polymerase Chain Reaction Method for α-Thalassemia Genotyping Using Capillary Electrophoresis

(2017) Basma Basha et al.   HEMOGLOBIN

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

(2017) Xuan Shang et al.   EBioMedicine

The prevalence of thalassemia in mainland China: evidence from epidemiological surveys

(2017) Ketong Lai et al.   Scientific Reports

Laboratory diagnosis of thalassemia

(2016) V. Brancaleoni et al.   International Journal of Laboratory Hematology

The molecular spectrum and distribution of haemoglobinopathies in Cyprus: a 20-year retrospective study

(2016) Petros Kountouris et al.   Scientific Reports

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

(2015) Sue Richards et al.   GENETICS IN MEDICINE

Iron-Deficiency Anemia

(2015) Clara Camaschella   NEW ENGLAND JOURNAL OF MEDICINE

IthaGenes: An Interactive Database for Haemoglobin Variations and Epidemiology

(2014) Petros Kountouris et al.   PLoS One

State of the art and new developments in molecular diagnostics for hemoglobinopathies in multiethnic societies

(2013) C. L. Harteveld   International Journal of Laboratory Hematology

Updates of the HbVar database of human hemoglobin variants and thalassemia mutations

(2013) Belinda Giardine et al.   NUCLEIC ACIDS RESEARCH

World Distribution, Population Genetics, and Health Burden of the Hemoglobinopathies

(2013) T. N. Williams et al.   Cold Spring Harbor Perspectives in Medicine

The Prevention of Thalassemia

(2013) A. Cao et al.   Cold Spring Harbor Perspectives in Medicine

Molecular characterization and clinical presentation of HKαα and anti-HKαα alleles in southern Chinese subjects

(2012) X Shang et al.   CLINICAL GENETICS

Development and evaluation of a reverse dot blot assay for the simultaneous detection of common alpha and beta thalassemia in Chinese

(2011) Min Lin et al.   BLOOD CELLS MOLECULES AND DISEASES

Alpha-thalassemia

(2011) Renzo Galanello et al.   GENETICS IN MEDICINE

Thalassaemia

(2011) Douglas R Higgs et al.   LANCET

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

(2010) F Xiong et al.   CLINICAL GENETICS

Carrier screening for Beta-thalassaemia: a review of international practice

(2010) Nicole E Cousens et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Beta-thalassemia

(2010) Antonio Cao et al.   GENETICS IN MEDICINE