TY - JOUR AU - Weatherall, D. J. AU - Clegg, J. B. PY - 1996 DA - 1996// TI - Thalassemia--a global public health problem JO - Nat Med VL - 2 UR - https://doi.org/10.1038/nm0896-847 DO - 10.1038/nm0896-847 ID - Weatherall1996 ER - TY - JOUR AU - Galanello, R. AU - Origa, R. PY - 2010 DA - 2010// TI - Beta-thalassemia JO - Orphanet J Rare Dis VL - 5 UR - https://doi.org/10.1186/1750-1172-5-11 DO - 10.1186/1750-1172-5-11 ID - Galanello2010 ER - TY - JOUR AU - Zhang, J. AU - Yan, J. AU - Zeng, F. PY - 2018 DA - 2018// TI - Recent Progress on genetic diagnosis and therapy for β-thalassemia in China and around the world JO - Hum Gene Ther VL - 29 UR - https://doi.org/10.1089/hum.2017.228 DO - 10.1089/hum.2017.228 ID - Zhang2018 ER - TY - JOUR AU - Asadov, C. AU - Alimirzoeva, Z. AU - Mammadova, T. AU - Aliyeva, G. AU - Gafarova, S. AU - Mammadov, J. PY - 2018 DA - 2018// TI - β-Thalassemia intermedia: a comprehensive overview and novel approaches JO - Int J Hematol VL - 108 UR - https://doi.org/10.1007/s12185-018-2411-9 DO - 10.1007/s12185-018-2411-9 ID - Asadov2018 ER - TY - JOUR AU - Vinciguerra, M. AU - Passarello, C. AU - Cassara, F. AU - Leto, F. AU - Cannata, M. AU - Calvaruso, G. AU - Renda, D. AU - Maggio, A. AU - Giambona, A. PY - 2018 DA - 2018// TI - Coheredity of a new silent mutation: c.-29G>T, with a severe beta-thal mutation in a patient with beta-thalassemia intermediate JO - Int J Lab Hematol VL - 40 UR - https://doi.org/10.1111/ijlh.12777 DO - 10.1111/ijlh.12777 ID - Vinciguerra2018 ER - TY - JOUR AU - Aliyeva, G. AU - Abdulalimov, E. AU - Asadov, C. AU - Mammadova, T. AU - Gafarova, S. AU - Guliyeva, Y. PY - 2018 DA - 2018// TI - First report of beta-thalassemia intermedia in a patient compound heterozygous for −92 (C>T) and codons 36/37 (−T) mutations JO - Hemoglobin VL - 12 UR - https://doi.org/10.1080/03630269.2018.1470534 DO - 10.1080/03630269.2018.1470534 ID - Aliyeva2018 ER - TY - JOUR AU - Agapidou, A. AU - King, P. AU - Ng, C. AU - Tsitsikas, D. A. PY - 2018 DA - 2018// TI - Double heterozygocity for hemoglobin C and beta thalassemia dominant: a rare case of thalassemia intermedia JO - Hematol Rep VL - 9 UR - https://doi.org/10.4081/hr.2017.7447 DO - 10.4081/hr.2017.7447 ID - Agapidou2018 ER - TY - JOUR AU - Kelkar, A. J. AU - Moses, A. PY - 2017 DA - 2017// TI - Thalassemia intermedia phenotype resulting from rare combination of c.46delT [Codon15 (−T)] mutation of beta globin gene and HPFH3 JO - Clin Case Rep VL - 5 UR - https://doi.org/10.1002/ccr3.990 DO - 10.1002/ccr3.990 ID - Kelkar2017 ER - TY - JOUR AU - Pavlou, E. AU - Phylactides, M. AU - Kyrri, A. AU - Kalogerou, E. AU - Makariou, C. AU - Georgiou, I. AU - Delta-thalassemia in Cyprus, K. M. PY - 2006 DA - 2006// JO - Hemoglobin VL - 30 UR - https://doi.org/10.1080/03630260600868006 DO - 10.1080/03630260600868006 ID - Pavlou2006 ER - TY - JOUR AU - Goonasekera, H. W. AU - Paththinige, C. S. AU - Dissanayake, V. H. W. PY - 2018 DA - 2018// TI - Population screening for Hemoglobinopathies JO - Annu Rev Genomics Hum Genet VL - 19 UR - https://doi.org/10.1146/annurev-genom-091416-035451 DO - 10.1146/annurev-genom-091416-035451 ID - Goonasekera2018 ER - TY - JOUR AU - Mansoori, H. AU - Asad, S. AU - Rashid, A. AU - Karim, F. PY - 2016 DA - 2016// TI - Delta beta thalassemia: a rare hemoglobin variant JO - Blood Res VL - 51 UR - https://doi.org/10.5045/br.2016.51.3.213 DO - 10.5045/br.2016.51.3.213 ID - Mansoori2016 ER - TY - JOUR AU - Lettre, G. PY - 2012 DA - 2012// TI - The search for genetic modifiers of disease severity in the beta-hemoglobinopathies JO - Cold Spring Harb Perspect Med VL - 2 UR - https://doi.org/10.1101/cshperspect.a015032 DO - 10.1101/cshperspect.a015032 ID - Lettre2012 ER - TY - JOUR AU - Rujito, L. AU - Basalamah, M. AU - Siswandari, W. AU - Setyono, J. AU - Wulandari, G. AU - Mulatsih, S. AU - Sofro, A. S. AU - Sadewa, A. H. AU - Sutaryo, S. PY - 2016 DA - 2016// TI - Modifying effect of XmnI, BCL11A, and HBS1L-MYB on clinical appearances: a study on beta-thalassemia and hemoglobin E/beta-thalassemia patients in Indonesia JO - Hematol Oncol Stem Cell Ther VL - 9 UR - https://doi.org/10.1016/j.hemonc.2016.02.003 DO - 10.1016/j.hemonc.2016.02.003 ID - Rujito2016 ER - TY - JOUR AU - Murad, H. AU - Moassas, F. AU - Jarjour, R. AU - Mukhalalaty, Y. AU - Al-Achkar, W. PY - 2014 DA - 2014// TI - Prenatal molecular diagnosis of beta-thalassemia and sickle cell anemia in the Syrian population JO - Hemoglobin. VL - 38 UR - https://doi.org/10.3109/03630269.2014.978455 DO - 10.3109/03630269.2014.978455 ID - Murad2014 ER - TY - JOUR AU - Murad, H. AU - Moasses, F. AU - Dabboul, A. AU - Mukhalalaty, Y. AU - Bakoor, A. O. AU - Al-Achkar, W. AU - Jarjour, R. A. PY - 2018 DA - 2018// TI - Geographical distribution of beta-globin gene mutations in Syria JO - Hematology VL - 23 UR - https://doi.org/10.1080/10245332.2018.1461291 DO - 10.1080/10245332.2018.1461291 ID - Murad2018 ER - TY - JOUR AU - Yassin, M. M. AU - Sirdah, M. M. AU - Haddad, R. M. AU - Lubbad, A. H. AU - Al-Yazji, M. S. PY - 2013 DA - 2013// TI - Genotype-phenotype characteristics of β thalassemia children in the Gaza strip, Palestine JO - J Genet Disor Genet Rep VL - 02 ID - Yassin2013 ER - TY - JOUR AU - Liu, N. AU - Xie, X. M. AU - Zhou, J. Y. AU - Li, R. AU - Liao, C. AU - Li, D. Z. PY - 2013 DA - 2013// TI - Analysis of delta-globin gene mutations in the Chinese population JO - Hemoglobin VL - 37 UR - https://doi.org/10.3109/03630269.2012.747965 DO - 10.3109/03630269.2012.747965 ID - Liu2013 ER - TY - JOUR AU - Fessas, P. AU - Loukopoulos, D. AU - Loutradi-Anagnostou, A. AU - Komis, G. PY - 1982 DA - 1982// TI - 'Silent' beta-thalassaemia caused by a 'silent' beta-chain mutant: the pathogenesis of a syndrome of thalassaemia intermedia JO - Br J Haematol VL - 51 UR - https://doi.org/10.1111/j.1365-2141.1982.tb02821.x DO - 10.1111/j.1365-2141.1982.tb02821.x ID - Fessas1982 ER - TY - JOUR AU - Orkin, S. H. AU - Antonarakis, S. E. AU - Loukopoulos, D. PY - 1984 DA - 1984// TI - Abnormal processing of beta Knossos RNA JO - Blood VL - 64 ID - Orkin1984 ER - TY - JOUR AU - Gurgey, A. AU - Balkan, H. AU - Irken, G. AU - Gumruk, F. AU - Altay, S. AU - Kalaycioglu, A. AU - Oner, C. AU - Oner, R. PY - 1997 DA - 1997// TI - Compound heterozygosity for hemoglobin Knossos [alpha 2 beta 2 27 (B9) ala-Ser] and IVS I-1 mutation JO - Turk J Pediatr VL - 39 ID - Gurgey1997 ER - TY - JOUR AU - Altay, C. AU - Gurgey, A. PY - 1990 DA - 1990// TI - Beta-thalassemia intermedia in Turkey JO - Ann N Y Acad Sci VL - 612 UR - https://doi.org/10.1111/j.1749-6632.1990.tb24293.x DO - 10.1111/j.1749-6632.1990.tb24293.x ID - Altay1990 ER - TY - JOUR AU - Keser, I. AU - Manguoglu, E. AU - Kayisli, O. AU - Yesilipek, A. AU - Luleci, G. PY - 2007 DA - 2007// TI - Combination of Hb Knossos [cod 27 (G-T)] and IVSII-745 (C-G) in a Turkish patient with beta-thalassemia major JO - Genet Test VL - 11 UR - https://doi.org/10.1089/gte.2006.0521 DO - 10.1089/gte.2006.0521 ID - Keser2007 ER - TY - STD TI - Sun M, Lou J, Zhao Y, Liu Y. Molecular and Hematological Characterization of Two Novel delta-Globin Gene Mutations Found in Chinese Individuals. Hemoglobin. 2018;42:132-134. ID - ref23 ER - TY - JOUR AU - Velasco-Rodriguez, D. AU - Alonso-Dominguez, J. M. AU - Gonzalez-Fernandez, F. A. AU - Villarrubia, J. AU - Ropero, P. AU - Martinez-Nieto, J. AU - Fuente, F. AU - Guillen, R. AU - Acedo, N. AU - Seri, C. PY - 2014 DA - 2014// TI - Cava F. Deltabeta-thalassemia trait: how can we discriminate it from beta-thalassemia trait and iron deficiency anemia? JO - Am J Clin Pathol VL - 142 UR - https://doi.org/10.1309/AJCPPBQ8UB1WHXTS DO - 10.1309/AJCPPBQ8UB1WHXTS ID - Velasco-Rodriguez2014 ER - TY - JOUR AU - Sahli, C. A. AU - Bibi, A. AU - Ouali, F. AU - Siala, H. AU - Fredj, S. H. AU - Othmani, R. AU - Ouenniche, F. AU - Cheour, M. AU - Fitouri, Z. AU - Becher, S. B. AU - Messaoud, T. PY - 2012 DA - 2012// TI - δ0-thalassemia in cis of β Knossos globin gene: first homozygous description in thalassemia intermedia Libyans and first combination with codon 39 (C → T) in thalassemia intermedia Tunisian patients JO - Clin Chem Lab Med VL - 50 UR - https://doi.org/10.1515/cclm-2012-0102 DO - 10.1515/cclm-2012-0102 ID - Sahli2012 ER - TY - JOUR AU - Olds, R. J. AU - Sura, T. AU - Jackson, B. AU - Wonke, B. AU - Hoffbrand, A. V. AU - Thein, S. L. PY - 1991 DA - 1991// TI - A novel delta 0 mutation in cis with Hb Knossos: a study of different genetic interactions in three Egyptian families JO - Br J Haematol VL - 78 UR - https://doi.org/10.1111/j.1365-2141.1991.tb04460.x DO - 10.1111/j.1365-2141.1991.tb04460.x ID - Olds1991 ER - TY - JOUR AU - Oner, R. AU - Birben, E. AU - Acar, C. AU - Oner, C. AU - Kara, A. AU - Gumruk, F. AU - Gurgey, A. AU - Altay, C. PY - 2000 DA - 2000// TI - Molecular analysis of turkish beta-thalassemia heterozygotes with normal Hb A2 levels JO - Hemoglobin VL - 24 UR - https://doi.org/10.3109/03630260008997527 DO - 10.3109/03630260008997527 ID - Oner2000 ER - TY - JOUR AU - Nasouhipur, H. AU - Banihashemi, A. AU - Youssefi Kamangar, R. AU - Akhavan-Niaki, H. PY - 2014 DA - 2014// TI - Hb Knossos: HBB:c.82G>T associated with HBB:c.315+1G>a Beta zero mutation causes thalassemia intermedia JO - Indian J Hematol Blood Transfus VL - 30 UR - https://doi.org/10.1007/s12288-014-0343-y DO - 10.1007/s12288-014-0343-y ID - Nasouhipur2014 ER - TY - JOUR AU - Aditya, R. AU - Verma, I. C. AU - Saxena, R. AU - Kaul, D. AU - Khanna, V. K. PY - 2006 DA - 2006// TI - Relation of Xmn-1 Polymorphism & Five Common Indian Mutations of Thalassaemia with phenotypic presentation in b-Thalassaemia JO - JK Sci VL - 8 ID - Aditya2006 ER - TY - JOUR AU - Pereira, C. AU - Relvas, L. AU - Bento, C. AU - Abade, A. AU - Ribeiro, M. L. AU - Manco, L. PY - 2015 DA - 2015// TI - Polymorphic variations influencing fetal hemoglobin levels: association study in beta-thalassemia carriers and in normal individuals of Portuguese origin JO - Blood Cells Mol Dis VL - 54 UR - https://doi.org/10.1016/j.bcmd.2015.02.001 DO - 10.1016/j.bcmd.2015.02.001 ID - Pereira2015 ER -