A novel δº mutation in cis with Hb Knossos: a study of different genetic interactions in three Egyptian families
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1991.tb04460.x/fullpdf
Reference25 articles.
1. Nonrandom association of polymorphic restriction sites in the -globin gene cluster
2. Structural study of hemoglobin Knossos, β27 (B9) Ala→Ser
3. Homozygous hemoglobin Knossos (alpha 2 beta 227(B9) Ala----Ser): a new variety of beta+-thalassemia intermedia associated with delta degree- thalassemia
4. Locus assignment of human a globin mutations by selective amplification and direct sequencing
5. ‘Silent’ β-thalassaemia caused by a ‘silent’ β-chain mutant: the pathogenesis of a syndrome of thalassaemia intermedia
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3. Hb Knossos (HBB: c.82G > T), β-globin CD 5 (−CT) (HBB: c.17_18delCT) and δ-globin CD 59 (−a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia;BMC Pediatrics;2019-02-18
4. Delta0-talasemia por inserción de 27 pares de bases en el gen δ-globina con descenso de los valores de hemoglobina A2;Medicina Clínica;2015-04
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