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Hemoglobin
international journal for hemoglobin research
Volume 29, 2005 - Issue 2
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Short Communication

Two New δ-Globin Mutations: Hb A2-Ninive [δ133(H11)Val → Ala] and A δ+-Thalassemia Mutation [− 31 (A → G)] in the Tata Box of the δ-Globin Gene

Hannes Frischknecht IMD Institute for Medical and Molecular Diagnostics Ltd., Zürich, SwitzerlandCorrespondence[email protected]
&
Fabrizio Dutly IMD Institute for Medical and Molecular Diagnostics Ltd., Zürich, Switzerland
Pages 151-154 | Received 26 Oct 2004, Accepted 17 Nov 2004, Published online: 07 Jul 2009

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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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Imen Moumni, Amine Zorai, Bechir Ben Daoued, Ikbel Mosbahi, Souheil Omar, Neziha Kaabachi, Koussay Dellagi & Salem Abbes. (2007) Hb A2-Pasteur-Tunis [δ59(E3)Lys→Asn, AAG→AAC]: A New δ Chain Variant Detected by DNA Sequencing in a Tunisian Carrier of the Codon 39 (C→T) β0-Thalassemia Mutation. Hemoglobin 31:1, pages 23-29.
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Articles from other publishers (1)

Abdulrahman Alsultan, Duyen A. Ngo, John J. Farrell, Idowu Akinsheye, Nadia Solovieff, Hazem A. Ghabbour, Amein Al‐Ali, Ahmed Alsuliman, Muneer Al‐Baghshi, Waleed Albu‐Ali, Mohammed Alabdulaali, Clinton T. Baldwin, Lindsay A. Farrer, Hong Luo, Efthymia Melista, Surinder Safaya, Maxwell NwaruJr.Jr., David H.K. Chui & Martin H. Steinberg. (2012) A functional promoter polymorphism of the δ‐globin gene is a specific marker of the Arab‐Indian haplotype. American Journal of Hematology 87:8, pages 824-826.
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