The relative levels of βAand βSmRNAs in Hb S heterozygotes and in patients with Hb S-β+-thalassaemia or Hb S-β+-HPFH combinations
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1994.tb04921.x/fullpdf
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1. Differences in Affinity of Variant β Chains for a Chains: A Possible Explanation for the Variation in the Percentages of β Chain Variants in Heterozygotes
2. Another Form of tie Hereditary Persistence of Fetal Hemoglobin (The Atlanta Type)?
3. High-performance liquid chromatographic separation of human haemoglobins
4. Subunit assembly of hemoglobin: an important determinant of hematologic phenotype
5. Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction
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1. A comparative study of Greek nondeletional hereditary persistence of fetal hemoglobin and β-thalassemia compound heterozygotes;Journal of Molecular Medicine;2001-12-18
2. The Biologic Implications of a Rare Hemoglobin Mutant That Decreases Oxygen Affinity;Pediatric Research;2001-01
3. HOMOZYGOSITY FOR Hb E-SASKATOON [β22(B4)Glu → Lys] IN A TURKISH PATIENT;Hemoglobin;2001-01
4. FORTY-FOUR YEARS (1955–1999) DEVOTED TO HEMOGLOBIN RESEARCH: TITUS H. J. HUISMAN (1923–1999);Hemoglobin;2001-01
5. Cryptic splice site activation during RNA processing of MLL/AF4 chimeric transcripts in infants with t(4;11) positive ALL;Gene;2000-04
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