Hydrops fetalis associated with homozygosity for hemoglobin Taybe (? 38/39 THR deletion) in newborn triplets
Author:
Publisher
Wiley
Subject
Hematology
Reference11 articles.
1. Molecular mechanisms of ?-thalassemias. In: editors. Disorders of hemoglobin. Cambridge: Cambridge University Press; 2001. p 431-469.
2. Hb H hydrops foetalis syndrome: a case report and review of literature
3. Hb H hydrops fetalis syndrome associated with the interaction of two common determinants of α thalassaemia (--MED /αTSaudi α)
4. Short Communication:HB Taybe: Description of Genetics and Laboratory Findings in an Israeli Arab Family
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