Aumento de fertilidade como eventual mecanismo de manutenção das altas freqüências de hemoglobinopatias no Brasil

Mazzi, Michelle Marcondes; Teixeira, Rosa Chelminsky; Magna, Luís Alberto; Ramalho, Antonio Sérgio.
J. bras. patol. med. lab ; 39(4): 289-294, 2003.
Artículo en Portugués | LILACS | ID: lil-354506

Documentos relacionados

  1. Bone Health Impairment in Patients with Hemoglobinopathies: From Biological Bases to New Possible Therapeutic Strategies.
  2. Reliability of hemoglobin A<sub>2</sub> value as measured by the Premier Resolution system for screening of ß-thalassemia carriers.
  3. First Report of Compound Heterozygosity for Hb S (<i>HBB</i>: c.20A>T) and Hb Haringey (<i>HBB</i>: c.131A>G).
  4. Effect of Assorted Globin Haplotypes and &#945;-Thalassemia on the Clinical Heterogeneity of Hb S-ß-Thalassemia.
  5. Splice Acceptor Mutation [<i>HBB</i>:c.93-2A > T] in a Patient with Hb S/ß<sup>0</sup>-Thalassemia.
  6. Genetic Background of ß-Thalassemia in Northeast Algeria with Assessment of the Thalassemia Severity Score and Description of a new ß<sup>0</sup>-Thalassemia Frameshift Mutation (<i>HBB</i>: c.374dup; p.Pro126Thrfs*15).
  7. Coinheritance of a Rare Nucleotide Substitution on the ß-Globin Gene and Other Known Mutations in the Globin Clusters: Management in Genetic Counseling.
  8. Compound Heterozygosity of ß-Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, India.
  9. Targeting fetal hemoglobin expression to treat ß hemoglobinopathies.
  10. Hb Rush (<i>HBB</i>: c.304G>C): A Rare Variant Hemoglobin Mimicking the Hb S (<i>HBB</i>: c.20A>T) Variant on High Performance Liquid Chromatography.