R. Talmaci, J. Traeger-synodinos, E. Kanavakis, D. Coriu, and L. Garrila, Scanning of ?-globin gene for identification of ?-thalassemia mutation in Romanian population, Journal of Cellular and Molecular Medicine, vol.12, issue.2, pp.232-240, 2004.
DOI : 10.1002/ajh.2830450316

D. Weatheral and J. Clegg, The Thalassemia Syndrome, Blackwell Science, 2001.

U. Francke, J. Celenstein, and S. Gartler, The occurrence of new mutants in the X-linked recessive Lesh-Nyhan disease, AM J Hum Genet, vol.28, pp.123-127, 1976.

G. Tadmouri, O. Bileno÷lu, S. Kantarci, H. Kayserili, P. Perrin et al., A rare mutation [IVS-I-130 (G-A)] in a Turkish ?-thalassemia major patient, American Journal of Hematology, vol.19, issue.4, pp.223-225, 2000.
DOI : 10.1002/(SICI)1096-8652(200004)63:4<223::AID-AJH10>3.0.CO;2-B

N. Olieveri, Thalassemias, New Engl J Med, vol.341, pp.99-109, 1999.
DOI : 10.1002/9780470987001.ch13

H. Najmabadi, S. Teimourian, T. Khatibi, M. Neishabury, F. Pourfarzad et al., Ampli¿cation refractory mutation system (ARMS) and reverse hybridization in the detection of thalassemia mutations, Arch Iran Med, vol.4, pp.165-170, 2001.

H. Abolghasemi, A. Amid, S. Zeinali, M. Radfar, P. Eshghi et al., Thalassemia in Iran, Journal of Pediatric Hematology/Oncology, vol.29, issue.4, pp.233-238, 2007.
DOI : 10.1097/MPH.0b013e3180437e02

R. Jones, Structural Studies of Aminoethylated Hemoglobins by Automatic Peptide Chromatography, Cold Spring Harbor Symposia on Quantitative Biology, vol.29, issue.0, p.297, 1964.
DOI : 10.1101/SQB.1964.029.01.032

A. Giambona, C. Passarello, G. Ruggery, R. D. Teresi, P. Anza et al., Analysis of -globin gene alleles in the Sicilian population: Identi¿cation of ¿ve new mutations, Haematologica, vol.91, pp.1681-1684, 2006.

T. Huisman and J. Jonxis, The Hemoglobinopathies: Techniques of Identification, 1977.

S. Miller, D. Dykes, and H. Polesky, A simple salting out procedure for extracting DNA from human nucleated cells, Nucleic Acids Research, vol.16, issue.3, p.1215, 1988.
DOI : 10.1093/nar/16.3.1215

J. Old, N. Varavalla, and D. Weatherall, Rapid detection and prenatal diagnosis of ??-thalassaemia: studies in Indian and Cypriot populations in the UK, The Lancet, vol.336, issue.8719, pp.834-837, 1990.
DOI : 10.1016/0140-6736(90)92338-I

D. Weatherall, J. Clegg, R. Gibbons, D. Higgs, N. Olieveri et al., Hereditary persistence of fetal hemoglobin, The Thalassemia Syndromes, pp.450-455, 2001.

S. Samuel, C. D. Chong, D. R. Boehm, G. R. Higgs, and . Cutting, Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemia, Blood, vol.95, pp.360-362, 2000.

H. Rannery, A. Jacobs, B. Ramot, T. Bradley, and . Jr, Hemoglobin NYU, a delta chain variant, ??2??212Lys, Journal of Clinical Investigation, vol.48, issue.11, pp.2057-2062, 1969.
DOI : 10.1172/JCI106171

M. Riberio, G. H. Buchanan-adair, I. Husman, and T. , Incorrect genetic counseling of a couple with -thalassemia, due to incomplete testing, Am J Hum Genet, vol.52, pp.842-843, 1993.

M. De-angioletti, G. Lacerra, C. Gaudiano, G. Mastrolonardo, L. Pagano et al., Epidemiology of the delta globin alleles in southern Italy shows complex molecular, genetic, and phenotypic features, Human Mutation, vol.393, issue.5, pp.358-367, 2002.
DOI : 10.1002/humu.10132

S. Eram, B. Azimifar, H. Abolghassemi, P. Fouladi, V. Lot¿ et al., GC)] Causes a Complex Prenatal Diagnosis in an Iranian Family, Hemoglobin, vol.89, issue.10, pp.289-292, 2005.
DOI : 10.1081/HEM-120005452