Haemoglobin H disease caused by alpha-thalassaemia and a new abnormal haemoglobin with an elongated alpha-chain (Hb constant spring) - abstract

Milner, Paul F. A; Weatherall, David J; Clegg, John B.
West Indian med. j ; 20(4): 266, Dec. 1971.
Artículo en Inglés | MedCarib | ID: med-6324

Documentos relacionados

  1. Third-generation sequencing identified a novel complex variant in a patient with rare alpha-thalassemia.
  2. CRISPR/Cas9 gene correction of HbH-CS thalassemia-induced pluripotent stem cells.
  3. Description of Hb Évora (<i>HBA2</i>: c.106T>C) on an Unexpected Allele in a Swiss Family.
  4. Mild &#945;-Thalassemia Caused by a Mosaic &#945;-Globin Gene Mutation.
  5. First Report of Nondeletional Hb H Disease Caused by an &#945;2-Globin Gene Mutation: <i>HBA2</i>: c.184A>T.
  6. Direct cord blood LAMP colorimetric phenol red assay for detecting &#945;<sup>0</sup>-thalassemia (SEA deletion); the validation and post-natal screening in Thailand.
  7. Hb Q-Thailand heterozygosity unlinked with the (-&#945;<sup>4.2</sup>/) &#945;<sup>+</sup>-thalassemia deletion allele identified by long-read SMRT sequencing: hematological and molecular analyses.
  8. Hb Hezhou [ß64(E8)Gly→Ser; <i>HBB</i>: c.193G>A]: A Novel Variant on the ß-Globin Gene.
  9. Life beyond alpha-thalassaemia: We are moving forward.
  10. Severe Hb H Disease Caused by Hb Zürich-Albisrieden (<i>HBA1</i>: c.178G>C): Another Case Report.