Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7-kb ?-globin gene deletion
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.2006.00771.x/fullpdf
Reference14 articles.
1. Sickle-cell disease
2. Universal Newborn Screening for Hb H Disease in California
3. Hemoglobinopathies mimicking Hb S/β-thalassemia: Hb S/S with α-thalassemia and Hb S/Volga
4. DNA sequence variation associated with elevated fetal G gamma globin production
5. The L1 family (Kpnl family) sequence near the 3' end of human β-globin gene may have been derived from an active L1 sequence
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