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Hemoglobin
international journal for hemoglobin research
Volume 27, 2003 - Issue 3
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SHORT COMMUNICATION

Identification of a New β-Thalassemia Nonsense Mutation [Codon 59 (AAG→TAG)]

Margie Patterson Hamilton Regional Laboratory Medicine Program, Hamilton, Ontario, Canada
,
Lynda Walker Hamilton Regional Laboratory Medicine Program, Hamilton, Ontario, Canada
,
David H. K. Chui Hamilton Regional Laboratory Medicine Program, Hamilton, Ontario, Canada; Department of Pathology and Molecular Medicine, McMaster University Medical Centre, Room 3N17, McMaster University Faculty of Health Sciences, 1200 Main St. West, Hamilton, Ontario, Canada, L8N 3Z5
,
Alan R. Cohen Children's Hospital of Philadelphia, Philadelphia, PennsylvaniaUSA
&
Dr. John S. Waye Hamilton Regional Laboratory Medicine Program, Hamilton, Ontario, Canada; Department of Pathology and Molecular Medicine, McMaster University Medical Centre, Room 3N17, McMaster University Faculty of Health Sciences, 1200 Main St. West, Hamilton, Ontario, Canada, L8N 3Z5
Pages 201-203 | Received 17 Jan 2003, Accepted 24 Mar 2003, Published online: 07 Jul 2009

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Xinping Chen, Zhangli Lin, Junjie Hu, Shiping Chen, Shu Wen, Aizhu Wu, Hong Wu, Jiali Huang, Hanqiang Wang, Jun Sun, Zhiyu Peng, Yan Sun & Shengmiao Fu. (2021) Report of Two Novel Thalassemia Variants, HBB: c.181delG and HBA1: c.121_126delAAGACC, in Chinese Individuals. Hemoglobin 45:1, pages 52-55.
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Hannes Frischknecht, Heinz Troxler, Fabrizio Dutly, Lynda Walker, Betty-Ann Hohenadel, Barry Eng & John S. Waye. (2010) Characterization of Three Novel δ Chain Hemoglobin Variants and Two δ-Thalassemia Alleles. Hemoglobin 34:4, pages 374-382.
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Hannes Frischknecht, Fabrizio Dutly, Lynda Walker, Lisa M. Nakamura-Garrett, Barry Eng & John S. Waye. (2009) Three New β-Thalassemia Mutations with Varying Degrees of Severity. Hemoglobin 33:3-4, pages 220-225.
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John S. Waye, Lynda Walker, Lisa M. Nakamura, Barry Eng & Andrew McFarlane. (2009) Hb North York [β117(G19)His→Asp]: A New β Chain Hemoglobin Variant. Hemoglobin 33:1, pages 51-53.
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Barry Eng, Lynda Walker, Lisa M. Nakamura, Carolyn Hoppe, Mahin Azimi, Helen Lee & John S. Waye. (2007) Three New β-Globin Gene Promoter Mutations Identified Through Newborn Screening. Hemoglobin 31:2, pages 129-134.
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Lynda Walker, Barry Eng, Andrew McFarlane & John S. Waye. (2007) High Oxygen Affinity Hemoglobin Variant in a Canadian Family: Hb Bunbury [β94(FG1)Asp→Asn, GAC→AAC]. Hemoglobin 31:1, pages 101-103.
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Antonio Amato, Maria Pia Cappabianca, Donatella Ponzini, Paola Di Biagio, Alessia Colosimo, Valentina Guida, Fabrizio Mastropietro, Enrica Foglietta, Paola Grisanti, Silvana Rinaldi, Bruno Dallapiccola & Ida Bianco. (2006) Detection of a Rare β-Globin Nonsense Mutation [Codon 59 (AAG→TAG)] in an Italian Family. Hemoglobin 30:3, pages 405-407.
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Lynda Walker, Margie Patterson, Barry Eng, Andrew McFarlane & John S. Waye. (2005) Identification of a New δ Chain Hemoglobin Variant in a β-Thalassemia Carrier: Hb A2-MUMC [δ13(A10)Ala → Asp]. Hemoglobin 29:4, pages 285-287.
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Lynda Walker, Andrew McFarlane, Margie Patterson, Barry Eng & John S. Waye. (2003) Hb Castilla [β32(B14)Leu → Arg] Caused by a De Novo Mutation. Hemoglobin 27:4, pages 253-256.
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Articles from other publishers (3)

Francesca Salvatori, Giulia Breveglieri, Cristina Zuccato, Alessia Finotti, Nicoletta Bianchi, Monica Borgatti, Giordana Feriotto, Federica Destro, Alessandro Canella, Eleonora Brognara, Ilaria Lampronti, Laura Breda, Stefano Rivella & Roberto Gambari. (2009) Production of β‐globin and adult hemoglobin following G418 treatment of erythroid precursor cells from homozygous β 0 39 thalassemia patients . American Journal of Hematology 84:11, pages 720-728.
Crossref
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallSwee Lay Thein & William G. Wood. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 323 356 .
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. Weatherall. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 321 322 .

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