Normal Hb A₂ β-Thalassemia Trait: Frameshift Mutation (HBB: c.187_251dup) in Cis with the Hb A_2’ δ-Globin Gene Missense Mutation (HBD: c.49G>C)

John S. WayeHamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada;Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, CanadaCorrespondence[email protected]

Barry EngHamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada

Laurie HellensHamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada

Betty-Ann HohenadelHamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada

Lisa M. NakamuraHamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada

Lynda WalkerHamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada

Normal Hb A₂ β-Thalassemia Trait: Frameshift Mutation (HBB: c.187_251dup) in Cis with the Hb A_2’ δ-Globin Gene Missense Mutation (HBD: c.49G>C)

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Normal Hb A2 β-Thalassemia Trait: Frameshift Mutation (HBB: c.187_251dup) in Cis with the Hb A2’ δ-Globin Gene Missense Mutation (HBD: c.49G>C)

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Normal Hb A₂ β-Thalassemia Trait: Frameshift Mutation (HBB: c.187_251dup) in Cis with the Hb A_2’ δ-Globin Gene Missense Mutation (HBD: c.49G>C)