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Hemoglobin
international journal for hemoglobin research
Volume 26, 2002 - Issue 3
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Original

IDENTIFICATION OF A COMPOUND β-THALASSEMIA HOMOZYGOSITY [CODON 10 (GC C→GC A) AND CODON 16 (—C)] IN AN AFGHAN FAMILY

Walter Krugluger Department of Clinical Chemistry, Municipal Hospital Rudolfstiftung, Juchgasse 25, Vienna, A-1030, Austria
&
Pierre Hopmeier Department of Clinical Chemistry, Municipal Hospital Rudolfstiftung, Juchgasse 25, Vienna, A-1030, Austria
Pages 317-320 | Received 09 Nov 2001, Accepted 14 Feb 2002, Published online: 07 Jul 2009

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Alice E. Gallienne, Nicola M. Iberson, Hélène M. Dréau, Helen Jackson, Patricia A. Bignell, John M. Old, Anna Schuh & Shirley J. Henderson. (2010) Characterization of a Novel Deletion Causing β-Thalassemia Major in an Afghan Family. Hemoglobin 34:1, pages 110-114.
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Roshan B. Colah, Anita Nadkarni, Aruna Pawar, Ajit Gorakshakar, Supriya Phanasgaonkar & Dipika Mohanty. (2003) Co‐existence of the Codon 16 (–C) (β0) and Codon 10 (C→A) (β+) Mutations on the Same β‐Globin Gene. Hemoglobin 27:2, pages 133-135.
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Articles from other publishers (1)

C Préhu, J Riou, J Henthorn & H Wajcman. (2007) A New Silent β Chain Variant: Hb Hounslow [β80(EF4)Asn→Tyr]. Balkan Journal of Medical Genetics 10:1, pages 29-32.
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