238 papers found
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Analysis Of δ-Globin Gene Mutations in the Chinese Population
Prenatal diagnosis of an atypical 1q21.1 microdeletion and duplication associated with foetal urogenital abnormalities
Third-trimester genetic amniocentesis in mainland China
Prenatal diagnosis and molecular characterization of a novel locus for Dandy–Walker malformation on chromosome 7p21.3
α0-Thalassemia Trait with Normal Red Cell Indices: A Report of Two Cases
Prenatal diagnosis of Cri du Chat syndrome: four cases report
Hb J-Wenchang-Wuming [α11(A9)Lys→Gln (AAG>CAG) (α2 or α1)] Compromises Neonatal Screening for α-Thalassemia with the Sebia Capillarys2 Electrophoresis System
Acceptability of supplementary QF-PCR among women undergoing prenatal diagnosis in mainland China
Prenatal diagnosis of trisomy 18: Report of 76 cases in a mainland Chinese hospital
A Novel Case of Hb Phnom Penh: Codons 117/118 (+ATC) as a Cause of α+-Thalassemia
Rapid Detection of Common Mutations of the FGFR3 Gene Causing Thanatophoric Dysplasia Type I: Two Case Reports
Association of Hb New York with Hb E and α0-Thalassemia in a Chinese Woman Identified by Sebia Capillarys2 System
A Novel α-Thalassemia Frameshift Mutation: Codon 8 (–C)
Screening for Common Nondeletional α-Thalassemias in Chinese Newborns by Determination of Hb Bart’s Using the Sebia Capillarys 2 Electrophoresis System
Screening for mutations in the α-globin genes leading to abnormal hemoglobin variants with high resolution melting analysis
出訪香港浸會大學暨澳門科技大學與澳門理工學院報告書
Cord Blood Analysis for Rapid Prenatal Confirmation of Hb Bart’s Disease Using the Sebia Capillary Electrophoresis System
Prenatal screening for Down syndrome in pregnancies at risk for α-thalassemia: CORRESPONDENCE
Early Prenatal Diagnosis of Thalassemia: The First Report of Experience in Mainland China
Phenotypic Variability in a Chinese Family with Nondeletional Hb H-Hb Quong Sze Disease
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