238 papers found
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Combination of Hb Heze [β144(HC1)Lys→Arg; HBB: c.434A>G] and β0-Thalassemia in a Chinese Patient with β-Thalassemia Intermedia
A Severe Case of Hemoglobin H Disease due to Compound Heterozygosity for Deletion of the Major α-Globin Regulatory Element (MCS-R2) and α0-Thalassemia
Increased first-trimester nuchal translucency associated with a dicentric chromosome and 9q34.3 microdeletion syndrome
Hb Alesha [β67(E11)Val→Met (GTG>ATG); HBB: c.202G > A] Found in a Chinese Girl
First Report of a Chinese Family Carrying a Double Heterozygosity for Hb Q-Thailand and Hb J-Bangkok
Prenatal diagnosis and early postnatal management of pyriform sinus cyst: experience at a single medical center in mainland China: Neonatal pyriform sinus cysts
Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (– –SEA/) Deletion
Incidental prenatal detection of DMD gene deletion using array comparative genomic hybridization
A Program on Noninvasive Prenatal Diagnosis of α-Thalassemia in Mainland China: A Cost–Benefit Analysis
Hb Dapu (HBA2: c.52G > T): A Novel Nondeletional α-Thalassemia Mutation
Mild Microcytic Anemia in an Infant with a Compound Heterozygosity for Hb C (HBB: c.19G > A) and Hb Osu Christiansborg (HBB: c.157G > A)
Maternal serum PlGF (placental growth factor) in Chinese women in the first trimester undergoing screening for Down syndrome
A New δ-Globin Gene Variant: Hb A2-Fengshun [δ121(GH4)Glu→Lys (HBD: c.364G > A)]
Prenatal diagnosis of thalassemia in twin pregnancies in mainland China
First Case of a Compound Heterozygosity for Two Nondeletionalα-Thalassemia mutations, Hb Constant Spring and Hb Quong Sze
Consequences of Delayed Prenatal Diagnosis of β-Thalassemia in Mainland China
定時制高校における効果的なデートDV予防授業の検討
Prenatal diagnosis of fetuses with increased nuchal translucency using an approach based on quantitative fluorescent polymerase chain reaction and genomic microarray
A novel selective deletion of the major α-globin regulatory element (MCS-R2) causing α-thalassaemia
Fetal Anemia and Hydrops Fetalis Associated with Homozygous Hb Constant Spring (HBA2: c.427T > C)
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