M. Jad, Thalassemia in Iran: epidemiology, prevention, and management, J Pediatr Hematol Oncol, vol.29, pp.233-238, 2007.

A. Ghavamzadeh, P. Nasseri, M. Eshraghian, M. Jahani, I. Baybordi et al., Prognostic factors in bone marrow transplantation for beta thalassemia major: experiences from Iran, Bone Marrow Transplantation, vol.22, issue.12, pp.1167-1169, 1998.
DOI : 10.1038/sj.bmt.1701509

Z. Rahimi, A. Merat, M. Haghshenass, H. Madani, M. Rezaei et al., Plasma lipids in Iranians with sickle cell disease: Hypocholesterolemia in sickle cell anemia and increase of HDL-cholesterol in sickle cell trait, Clinica Chimica Acta, vol.365, issue.1-2, pp.217-220, 2006.
DOI : 10.1016/j.cca.2005.08.022

A. Chan, C. So, E. Ma, and L. Chan, A laboratory strategy for genotyping haemoglobin H disease in the Chinese, Journal of Clinical Pathology, vol.60, issue.8, pp.931-934, 2007.
DOI : 10.1136/jcp.2006.042242

H. Shih, T. Er, T. Chang, Y. Chang, T. Liu et al., Development of a high-resolution melting method for the detection of hemoglobin alpha variants, Clinical Biochemistry, vol.43, issue.7-8, pp.671-676, 2010.
DOI : 10.1016/j.clinbiochem.2010.01.011

P. Zamaro and C. Bonini-domingos, Short Communication Abnormal hemoglobin phenotypes in carriers of mild anemia in Latin America, Genetics and Molecular Research, vol.9, issue.1, pp.425-428, 2010.
DOI : 10.4238/vol9-1gmr721

V. Hadavi, A. Taromchi, M. Malekpour, B. Gholami, H. Law et al., Elucidating the spectrum of ??-thalassemia mutations in Iran, Haematologica, vol.92, issue.7, pp.992-993, 2007.
DOI : 10.3324/haematol.10658

S. Miller, D. Dykes, H. Polesky, D. Bowden, M. Vickers et al., A simple salting out procedure for extracting DNA from human nucleated cells A PCR-based strategy to detect the common severe determinants of alpha thalassaemia, Nucleic Acids Res. Br J Haematol, vol.16, issue.81, pp.1215104-108, 1988.

F. Sanger, S. Nicklen, and A. Coulson, DNA sequencing with chain-terminating inhibitors, Proceedings of the National Academy of Sciences, vol.74, issue.12, pp.104-108, 1977.
DOI : 10.1073/pnas.74.12.5463
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC431765

R. Hardison, D. Chui, B. Giardine, C. Riemer, G. Patrinos et al., HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server, Human Mutation, vol.25, issue.3, pp.225-233, 2002.
DOI : 10.1002/humu.10044

Y. Huang, M. Lin, J. Wu, L. Yang, and Z. Xiang, Hb CS-H disease combined with ??-thalassemia-a case report, Blood Cells, Molecules, and Diseases, vol.44, issue.4, pp.215-216, 2010.
DOI : 10.1016/j.bcmd.2010.01.003

C. Harteveld, J. Traeger-synodinos, A. Ragusa, M. Fichera, E. Kanavakis et al., Different geographic origins of Hb Constant Spring [alpha(2) codon 142 TAA-->CAA]. Haematologica2001, pp.36-38

Z. Rahimi, M. Rezaei, R. Nagel, and A. Muniz, Molecular and hematologic analysis of hemoglobin Q-Iran and hemoglobin Setif in Iranian families, Arch Iran Med, vol.11, pp.382-386, 2008.

G. Nozari, S. Rahbar, P. Darbre, and H. Lehmann, Hemoglobin Setif (??94 (G1) ASP ??? TYR) in Iran a Report of 9 Cases, Hemoglobin, vol.400, issue.3, p.289, 1977.
DOI : 10.3109/03630267709003412

G. Schiliro, G. Russo-mancuso, S. Dibenedetto, P. Samperi, A. Cataldo et al., Six Rare Hemoglobin Variants Found in Sicily, Hemoglobin, vol.25, issue.5, pp.431-437, 1991.
DOI : 10.3109/03630269108998862

G. Dinçol, D. Elam, A. Kutlar, and F. Kutlar, Hb Setif [ 94 (G1) Asp Tyr ( 2)] detected in a Turkish family, pp.249-252, 2003.

A. Kyrri, X. Felekis, E. Kalogerou, B. Wild, L. Kythreotis et al., Hemoglobin Variants in Cyprus, Hemoglobin, vol.114, issue.2, pp.81-94, 2009.
DOI : 10.3109/03630267809007068

Z. Rahimi, A. Muniz, and H. Mozafari, Abnormal hemoglobins among Kurdish population of Western Iran: hematological and molecular features, Molecular Biology Reports, vol.13, issue.3, pp.51-57, 2010.
DOI : 10.1007/s11033-009-9516-4

B. Al-awamy, G. Niazi, M. Naeem, J. Wilson, and T. Huisman, in a Saudi Newborn, Hemoglobin, vol.179, issue.2, pp.183-186, 1985.
DOI : 10.3109/03630268508997001

J. Clegg, D. Weatherall, I. Contopolou-griva, K. Caroutsos, P. Poungouras et al., Haemoglobin Icaria, a new chain-termination mutant with causes alpha thalassaemia, Nature. Br J Haematol, vol.251, issue.75, pp.245-247250, 1974.

E. Kanavakis, J. Traeger-synodinos, I. Papasotiriou, C. Vrettou, A. Metaxotou-mavromati et al., The interaction of alpha zero thalassaemia with Hb Icaria: three unusual cases of haemoglobinopathy H, A12) Trp leads to Arg. A variant hemoglobin associ ated with alpha-thalassemia-2, pp.332-33565, 1983.

G. Honig, M. Shamsuddin, L. Vida, M. Mompoint, E. Valcourt et al., An unstable alpha-chain variant expressed as alpha-thalassemia, Hemoglobin Evanston J Clin Invest, vol.14, issue.73, pp.1740-1749, 1984.
DOI : 10.1172/jci111382
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC437086

C. Harteveld, P. Wijermans, J. De-ree, T. Hal, P. Van-delft et al., A New Hb Evanston Allele [??14(A12)Trp ??? Arg] Found Solely, and in the Presence of Common ?????Thalassemia Deletions, in Three Independent Asian Cases, Hemoglobin, vol.87, issue.1, pp.1-5, 2004.
DOI : 10.1081/HEM-120028881

R. Das, G. Garewal, R. Shaji, J. Ahluwalia, H. Bali et al., Investigation of persistent hypochromic microcytosis unmasks hemoglobin Evanston [?? 14 (A12) Try ??? Arg] in a patient of cyclic thrombocytopenia preceding Takayasu's disease, Hematology, vol.119, issue.4, pp.427-429, 2005.
DOI : 10.1093/rheumatology/39.3.337

N. Al-allawi, A. Badi, H. Imanian, N. Nikzat, J. Jubrael et al., Molecular Characterization of ??-Thalassemia in the Dohuk Region of Iraq, Hemoglobin, vol.100, issue.1, pp.37-44, 2009.
DOI : 10.1081/HEM-47019

E. Ma, A. Chan, and A. Lee, ; (??2)] in a Chinese Family, Hemoglobin, vol.88, issue.5, pp.213-216, 2004.
DOI : 10.1111/j.1365-2141.1990.tb07884.x

H. Wajcman, J. Kister, M. Rad, A. Marden, M. Riou et al., Hb Val de Marne [alpha 133(H16)Ser-->Arg]: a new hemoglobin variant Hemoglobin, pp.407-417, 1993.

C. Harteveld, P. Giordano, M. Losekoot, J. Heister, D. Batelaan et al., -chain variant associated with a mild alpha-thalassaemic phenotype, Br J Haematol, vol.94, issue.2, pp.129483-485, 1996.
URL : https://hal.archives-ouvertes.fr/hal-00315124

C. Suarez, D. Jue, and W. Moo-penn, Hemoglobin Savaria--alpha 49(CE7)Ser----Arg in the United States, pp.627-629, 1985.

P. Ojwang, T. Ogada, B. Webber, J. Wilson, and T. Huisman, in an Indigenous Female from Kenya, Hemoglobin, vol.4, issue.2, pp.197-200, 1985.
DOI : 10.3109/03630268508997004

J. Szelenyi, M. Horanyi, J. Foldi, J. Hudacsek, L. Istvan et al., A New Hemoglobin Variant in Hungary: Hb Savaria-??49 (CE7) Ser+Arg, Hemoglobin, vol.218, issue.1, pp.27-38, 1980.
DOI : 10.3109/03630268009042371

D. Juricic, G. Efremov, J. Wilson, and T. Huisman, in a Yugoslavian Family, Hemoglobin, vol.179, issue.6, pp.631-633, 1985.
DOI : 10.3109/03630268508997046

S. Henderson, M. Pitman, J. Mccarthy, A. Molyneux, and J. Old, Molecular prenatal diagnosis of Hb H hydrops fetalis caused by haemoglobin Adana and the implications to antenatal screening for alpha-thalassaemia

M. Curuk, A. Dimovski, E. Baysal, L. Gu, F. Kutlar et al., Hb adana or ??259(E8)Gly???Asp??2, A severely unstable ??1-globin variant, observed in combination with the -(??)20.5 KB ??-thal-1 deletion in two Turkish patients, American Journal of Hematology, vol.41, issue.4, pp.270-275, 1993.
DOI : 10.1002/ajh.2830440410

K. Mcbride, K. Snow, K. Kubik, V. Fairbanks, J. Hoyer et al., Hb DARTMOUTH [??66(E15)Leu ??? Pro (??2) (CTG ??? CCG)]: A NOVEL ??2-GLOBIN GENE MUTATION ASSOCIATED WITH SEVERE NEONATAL ANEMIA WHEN INHERITED IN TRANS WITH SOUTHEAST ASIAN ??-THALASSEMIA-1, Hemoglobin, vol.7, issue.2, pp.375-382, 2001.
DOI : 10.1111/j.1600-0609.1986.tb01734.x