Hydrops fetalis associated with homozygosity for hemoglobin Taybe (α 38/39 THR deletion) in newborn triplets

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1α-Thalassemia Caused by a 16 BP Deletion in the 3′ Untranslated Region of the α2-Globin Gene Including the First Nucleotide of the Poly a Signal Sequence1997 · 10 citations
2. 2Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia2000 · 474 citations
3. 3Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care Problem1998 · 268 citations
4. 4Compound heterozygosity for two α‐globin gene defects, Hb taybe (α1; 38 or 39 minus thr) and a poly a mutation (α2; AATAAA → AATAAG), results in a severe hemolytic anemia1994 · 28 citations
5. 5Hb H hydrops fetalis syndrome associated with the interaction of two common determinants of α thalassaemia (‐‐MED/αTSaudiα)2002 · 42 citations