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Hemoglobin
international journal for hemoglobin research
Volume 30, 2006 - Issue 3
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SHORT COMMUNICATION

Hb Sallanches [α104(G11)Cys→Tyr, TGC→TAC (α2)]: An Unstable Hemoglobin Variant Found in an Indian Child

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Pages 393-396 | Received 09 Dec 2005, Accepted 27 Jan 2006, Published online: 07 Jul 2009

REFERENCES

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  • Morle F, Francina A, Ducrocq R, Wajcman H, Gonnet C, Philippe N, Souillet G, Godet J. A new α chain variant Hb Sallanches [α104(G11)Cys→Tyr] associated with Hb H disease in one homozygous patient. Br J Haematol 1995; 91(3)608–611, [INFOTRIEVE]
  • Waye JS, Walker L, Chui DHK, Lafferty J, Kirby M. Homozygous Hb Sallanches [α104(G11)Cys→Tyr] in a Pakistani child with Hb H disease. Hemoglobin 2000; 24(4)355–357, [INFOTRIEVE]
  • Khan SN, Butt FI, Riazuddin S, Galanello R. Hb Sallanches [α104(G11)Cys→Tyr]: a rare α2-globin chain variant found in the homozygous state in three members of a Pakistani family. Hemoglobin 2000; 24(1)31–35, [INFOTRIEVE]

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