Frequency and Quantitative Levels ofTγ Chain (Hb F Sardinia) in the Fetal Hemoglobin of Newborn and Fetuses
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630268008996227
Reference22 articles.
1. Evidence for multiple structural genes for the gamma chain of human fetal hemoglobin.
2. The chemical heterogeneity of the fetal hemoglobin in normal newborn infants and in adults
3. A New Hb Variant: Hb F Sardinia γ75 (e 19) Isoieucine→Threonine Found in a Family with Hb G Philadelphia, β-Chain Deficiency and a Lepore-Like Haemoglobin Indistinguishable from Hb A2
4. Significance of a new type of human fetal hemoglobin carrying a replacement isoleucine ? threonine at position 75 (E 19) of the ? chain
5. Polymorphisms of human γ-globin genes in Mediterranean populations
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1. Hemoglobin tilburg: α2-ß2 73 (E 17) Asp→Gly;Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology;1988-11
2. Hematological Values of 163 Normal Fetuses between 18 and 30 Weeks of Gestation;Pediatric Research;1986-04
3. The Gamma Globin Chain Heterogeneity of the Sardinian Newborn Baby;Hemoglobin;1986-01
4. Development of a screening system for detection of somatic mutations. II. The use of peptides and insoluble protein fragments in a non-competitive solid-phase enzyme immunoassay;Journal of Immunological Methods;1983-05
5. Hb F-Siena (α2Aγt2121 (Gh4) Glu→Lys). A New Fetal Hemoglobin Variant;Hemoglobin;1983-01
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