REFERENCES
- Brotherton TW, Chui DHK, Gauldie J, Patterson M. Hemoglobin ontogeny during normal mouse fetal development. Proc Natl Acad Sci USA 1979; 76(6)2853–2857, [PUBMED], [INFOTRIEVE]
- Walker L, Patterson M, Eng B, McFarlane A, Waye JS. Identification of a new δ chain hemoglobin variant in a β-thalassemia carrier: Hb A2-MUMC [δ13(A10)Ala→Asp]. Hemoglobin 2005; 29(4), [CROSSREF]
- Patterson M, Walker L, Eng B, Waye JS. High Hb A2 β-thalassemia due to a 468 bp deletion in a patient with Hb S/β-thalassemia. Hemoglobin 2005; 29(4), [CROSSREF]
- Eng B, Walsh R, Walker L, Patterson M, Waye JS. Characterization of a rare single α-globin gene deletion in a Chinese woman with Hb H disease. Hemoglobin 2005; 29(4), [CROSSREF]