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α -Thalassemia Trait Caused by Frameshift Mutations in Exon 2 of the α 2-Globin Gene: HBA2:c.131delT and HBA2:c.143delA

✍ Scribed by Finlayson, Jill; Ghassemifar, Reza; Holmes, Paula; Grey, Dianne; Newbound, Christopher; Pell, Nicole; Jennens, Michelle; Greenwood, Laura; Beilby, John

Book ID: 115527295
Publisher: Informa plc
Year: 2012
Tongue: English
Weight: 289 KB
Volume: 36
Category: Article
ISSN: 0363-0269
DOI: 10.3109/03630269.2012.717053

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To the Editor: Trisomy 21 Down's syndrome (DS) predisposes to the development of acute lymphocytic and non-lymphocytic leukemias [ 1-31, acute myelofibrosis [4], and a transient myeloproliferative disorder of newborns [Z]. The hypereosinophilic syndrome (HES) is a myeloproliferative Department of Me