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Hemoglobin
international journal for hemoglobin research
Volume 25, 2001 - Issue 4
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Original

IDENTIFICATION OF TWO NEW α-THALASSEMIA MUTATIONS IN EXON 2 OF THE α1-GLOBIN GENE

Dr. John S. Waye Department of Pathology and Molecular Medicine, McMaster University Medical Centre, 1200 Main Street West, Hamilton, Ontario, L8N 3Z5, Canada; Hamilton Regional Laboratory Medicine Program, Provincial Hemoglobinopathy and DNA Diagnostic Laboratory, Hamilton, Ontario, L8N 3Z5, Canada
,
Barry Eng Hamilton Regional Laboratory Medicine Program, Provincial Hemoglobinopathy and DNA Diagnostic Laboratory, Hamilton, Ontario, L8N 3Z5, Canada
,
Margaret Patterson Hamilton Regional Laboratory Medicine Program, Provincial Hemoglobinopathy and DNA Diagnostic Laboratory, Hamilton, Ontario, L8N 3Z5, Canada
,
Manuel D. Carcao The Hospital for Sick Children, Toronto, Ontario, M5G 1X8, Canada
,
Lebe Chang The Hospital for Sick Children, Toronto, Ontario, M5G 1X8, Canada
,
Nancy F. Olivieri The Hospital for Sick Children, Toronto, Ontario, M5G 1X8, Canada
&
David H. K. Chui Hamilton Regional Laboratory Medicine Program, Provincial Hemoglobinopathy and DNA Diagnostic Laboratory, Hamilton, Ontario, L8N 3Z5, Canada
 show all
Pages 391-396 | Received 27 Apr 2000, Accepted 18 Jun 2001, Published online: 07 Jul 2009

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Samaneh Farashi, Negin Faramarzi Garous, Fatemeh Zeinali, Shadi Vakili, Mehri Ashki, Hashem Imanian, Hossein Najmabadi, Azita Azarkeivan & Ahmad Tamaddoni. (2015) A 21 Nucleotide Duplication on the α1- and α2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease. Hemoglobin 39:3, pages 196-200.
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Varvara Douna, Dimitra Liapi, Dimitrios Kampourakis, Zoe Repapinou, Ioannis Papassotiriou, Alexandra Stamoulakatou, Christos Poziopoulos, Emmanuel Kanavakis & Joanne Traeger-Synodinos. (2008) First Observation of Hb Taybe [Codons 38/39 (−Acc) Thr→0 (α1)] In Greece: Clinical and Hematological Findings in Patients With Co-Inherited α+-Thalassemia Mutations. Hemoglobin 32:4, pages 371-378.
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Henri Wajcman, Jan Traeger-Synodinos, Ioannis Papassotiriou, Piero C. Giordano, Cornelis L. Harteveld, Véronique Baudin-Creuza & John Old. (2008) Unstable and Thalassemic α Chain Hemoglobin Variants: A Cause of Hb H Disease and Thalassemia Intermedia. Hemoglobin 32:4, pages 327-349.
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Gerasimos Dimisianos, Joanne Traeger‐Synodinos, Christina Vrettou, Ioannis Papassotiriou & Emmanuel Kanavakis. (2004) A Rare 33 bp In‐Frame Deletion (α63–74 or α64–74 or α65–75) in the α1‐Globin Gene Causing α+‐Thalassemia: A Second Observation. Hemoglobin 28:2, pages 137-143.
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Articles from other publishers (3)

Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. Weatherall. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 241 265 .
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallDouglas R. Higgs. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 239 240 .
Nahid Tayebi, Barbara K. Stubblefield, Joseph K. Park, Eduard Orvisky, Jamie M. Walker, Mary E. LaMarca & Ellen Sidransky. (2003) Reciprocal and Nonreciprocal Recombination at the Glucocerebrosidase Gene Region: Implications for Complexity in Gaucher Disease. The American Journal of Human Genetics 72:3, pages 519-534.
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