238 papers found
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Noninvasive prenatal testing: impact on invasive prenatal diagnosis at a mainland Chinese tertiary medical center
Analysis of Fetal Blood: Is There Still a Role for Prenatal Diagnosis of Thalassemia?
First Detection of the −27 (A > G) (HBB: c.-77A > G) Mutation of theβ-Globin Gene in a Chinese Family
The Codon 35 (A > G) (HBB: c.107A > G) at theα-βChain Interface of theβ-Globin Gene: A Silent Mutation?
Non-invasive prenatal detection of haemoglobin Bart's disease by cardiothoracic ratio during the first trimester
The Frequency of α-Globin Gene Triplication in a Southern Chinese Population
Evidence of Selection for theα-Globin Gene Deletions and Triplications in a Southern Chinese Population
Frequencies of HKααand anti-HKααAlleles in Chinese Carriers of Silent Deletionalα-Thalassemia
Prevention of Hb Bart’s (γ4) Disease Associated with the – –THAIα0-Thalassemia Deletion in Mainland China
First-trimester combined screening for trisomy 21 in women at risk for α -thalassemia
Thalassemia Intermedia Caused by 16p13.3 Sectional Duplication in a β-Thalassemia Heterozygous Child
Compound Heterozygosity for HKααand anin CisDeletion of DoubleαGenes Presents asα-Thalassemia Trait
A Novel Mutation of Ribosomal Protein S19 Gene in a Chinese Child with Diamond-Blackfan Anemia
Association of an α-Globin Gene Cluster Duplication and Heterozygous β-Thalassemia in a Patient with a Severe Thalassemia Syndrome
Identification of Nondeletionalα-Thalassemia in a Prenatal Screening Program by Reverse Dot-Blot in Southern China
Prenatal diagnosis of 17q12 duplication and deletion syndrome in two fetuses with congenital anomalies
Delineation of the molecular basis of borderline hemoglobin A2 in Chinese individuals
Early Onset of Fetal Hydrops Associated with the α-Thalassemia – –THAIDeletion
Prenatal Control of Hb Bart’s Disease in Mainland China: Can We Do Better?
Co-inheritance of -thalassaemia and -thalassaemia in a prenatal screening population in mainland China
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