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Hemoglobin
international journal for hemoglobin research
Volume 27, 2003 - Issue 1
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Hb H Disease Among Tunisians: Molecular Characterization of α‐Thalassemia Determinants and Hematological Findings

Amine Zorai Hemoglobin Group, Laboratory of Hematology, Pasteur Institute, P.O. Box 74, Place du Belvedere, 1002, Tunis, Tunisia
,
Salem Abbes Hemoglobin Group, Laboratory of Hematology, Pasteur Institute, P.O. Box 74, Place du Belvedere, 1002, Tunis, Tunisia; Department of Biochemistry, Faculty of Medicine, Tunis, Tunisia
,
Claude Préhu Unité 468 de l'INSERM, Hôpital Henri Mondor, Créteil, France
,
Souheil Omar Department of Biochemistry, Faculty of Medicine, Tunis, Tunisia
,
Nathalie Gerard Unité 458 de l'INSERM, Hôpital Robert Debré, Paris, France
,
Raouf Hafsia Laboratory of Hematology, Aziza Othmana Hospital, Tunis, Tunisia
,
Bouaziz Asma Pediatric Service, Tahar Maamouri Hospital, Nabeul, Tunisia
,
Fethi Guemira Department of Biochemistry, Faculty of Medicine, Tunis, Tunisia
&
Kousay Dellagi Hemoglobin Group, Laboratory of Hematology, Pasteur Institute, P.O. Box 74, Place du Belvedere, 1002, Tunis, Tunisia
 show all
Pages 57-61 | Received 19 Sep 2002, Accepted 11 Oct 2002, Published online: 07 Jul 2009

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Arwa Z. Al-Riyami, Shahina Daar, Salam Al Kindi, Ali Al Madhani, Yasser Wali, Mohammed Al Rawahi & Shoaib Al Zadjali. (2020) α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region. Hemoglobin 44:1, pages 20-26.
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Nima Hafezi-Nejad, Mohsen Khosravi, Nooshin Bayat, Ariana Kariminejad, Valeh Hadavi, Christian Oberkanins, Azita Azarkeivan & Hossein Najmabadi. (2014) Characterizing a Cohort of α-Thalassemia Couples Collected During Screening for Hemoglobinopathies: 14 Years of an Iranian Experience. Hemoglobin 38:3, pages 153-157.
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Amel Haj Khelil, Sabri Denden, Nadia Leban, Houria Daimi, Ramzi Lakhdhar, Gérard Lefranc, Jemni Ben Chibani & Pascale Perrin. (2010) Hemoglobinopathies in North Africa: A Review. Hemoglobin 34:1, pages 1-23.
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Hamida Mesbah-Amroun, Fatiha Rouabhi, Rolande Ducrocq & Jacques Elion. (2008) Molecular Basis of α-Thalassemia in Algeria. Hemoglobin 32:3, pages 273-278.
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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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Majid Yavarian, Mehran Karimi, Amine Zorai, Cornelis L Harteveld & Piero C Giordano. (2005) Molecular Basis of Hb H Disease in Southwest Iran. Hemoglobin 29:1, pages 43-50.
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Articles from other publishers (3)

A. Zorai, I. Moumni, I. Mosbahi, K. Douzi, D. Chaouachi, F. Guemira & S. Abbes. (2015) Rare hemoglobin variants in Tunisian population. International Journal of Laboratory Hematology 37:2, pages 148-154.
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Rinini DastidarBani GajraMadhusnata De. (2011) Molecular and Hematological Characterization of Hemoglobin H Disease in the Bengali Population of Kolkata, India. Genetic Testing and Molecular Biomarkers 15:1-2, pages 93-96.
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H. Siala, F. Ouali, T. Messaoud, A. Bibi & S. Fattoum. (2008) α-Thalassaemia in Tunisia: some epidemiological and molecular data. Journal of Genetics 87:3, pages 229-234.
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