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Hemoglobin
international journal for hemoglobin research
Volume 29, 2005 - Issue 4
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Short Communication

High Hb A2 β-Thalassemia Due to a 468 bp Deletion in a Patient with Hb S/β-Thalassemia

Margie Patterson Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada
,
Lynda Walker Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada
,
Barry Eng Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada
&
Dr. John S. Waye Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, CanadaCorrespondence[email protected]
Pages 293-295 | Received 10 Jun 2005, Accepted 10 Jul 2005, Published online: 07 Jul 2009

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John S. Waye, Meredith Hanna, Betty-Ann Hohenadel, Lisa Nakamura, Lynda Walker & Barry Eng. (2017) Characterization of Two Novel Deletions Involving the 5′ Region of the β-Globin Gene. Hemoglobin 41:4-6, pages 239-242.
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. (2006) In Memoriam. Hemoglobin 30:1, pages 1-2.
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Articles from other publishers (4)

Martin H. Steinberg & Griffin P. Rodgers. (2015) HbA 2 : biology, clinical relevance and a possible target for ameliorating sickle cell disease . British Journal of Haematology 170:6, pages 781-787.
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Paula J. Griffin, Paola Sebastiani, Heather Edward, Clinton T. Baldwin, Mark T. Gladwin, Victor R. Gordeuk, David H.K. Chui & Martin H. Steinberg. (2014) The genetics of hemoglobin A 2 regulation in sickle cell anemia . American Journal of Hematology 89:11, pages 1019-1023.
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Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallMartin H. Steinberg. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 564 586 .
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallMartin H. Steinberg. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 435 436 .

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