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Azam Azimi, Parham Nejati, Soosan Tahmasebi, Sasan Alimoradi & Reza Alibakhshi. (2019) Characterization of the IVS-II-821 (A>C) (HBB: c.316-30A>C) Mutation in a β-Thalassemia Phenotype in Iran. Hemoglobin 43:1, pages 23-26.
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Masoumeh Jalilian, Farid Azizi Jalilian, Leila Ahmadi, Razieh Amini, Hossein Esfehani, Maryam Sosanian, Bahareh Rabbani, Majid Maleki & Nejat Mahdieh. (2017) The Frequency of HBB Mutations Among β-Thalassemia Patients in Hamadan Province, Iran. Hemoglobin 41:1, pages 61-64.
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Fakher Rahim, Bijan Kaikhaei, Khodamorad Zandian & Ashraf Hoseini. (2008) Co-inheritance of α-and β-thalassemia in Khuzestan Province, Iran. Hematology 13:1, pages 59-64.
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Amina Bibi, Taieb Messaoud, Cherif Beldjord & Slaheddine Fattoum. (2006) Detection of Two Rare β-Thalassemia Alleles Found in the Tunisian Population: Codon 47 (+A) and Codons 106/107 (+G). Hemoglobin 30:4, pages 437-447.
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Amina Bibi, Taieb Messaoud & Slaheddine Fattoum. (2006) Haplotypes Linked to Three Rare β-Thalassemia Mutations, Originally Reported in Tunisia. Hemoglobin 30:2, pages 175-181.
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Dongzhi Li, Can Liao, Jian Li & Xuewei Tang. (2006) The Codon 37 (TGG→TAG) β0-Thalassemia Mutation Found in a Chinese Family. Hemoglobin 30:2, pages 171-173.
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Hua Cao. (2004) Pharmacological Induction of Fetal Hemoglobin Synthesis using Histone Deacetylase Inhibitors. Hematology 9:3, pages 223-233.
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Slaheddine Fattoum, Taeib Messaoud & Amina Bibi. (2004) Molecular Basis of β‐Thalassemia in the Population of Tunisia. Hemoglobin 28:3, pages 177-187.
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Ajit C. Gorakshakar, Supriya P. Phanasgaonkar, Anita H. Nadkarni, Roshan B. Colah & Dipika Mohanty. (2004) Detection of Rare β‐Thalassemia Mutations by Denaturing Gradient Gel Electrophoresis Among Indians. Hemoglobin 28:1, pages 15-24.
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Mahmoud Abd El-Latif, Dvora Filon, Deborah Rund, Ariella Oppenheim & Moien Kanaan. (2002) THE β+-IVS-I-6 (T → C) MUTATION ACCOUNTS FOR HALF OF THE THALASSEMIA CHROMOSOMES IN THE PALESTINIAN POPULATIONS OF THE MOUNTAIN REGIONS. Hemoglobin 26:1, pages 33-40.
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Hossein Najmabadi, Roxana Karimi-Nejad, Solmaz Sahebjam, Farzin Pourfarzad, Shahram Teimourian, Farhad Sahebjam, Naser Amirizadeh & Mohammad H. Karimi-Nejad. (2001) THE β-THALASSEMIA MUTATION SPECTRUM IN THE IRANIAN POPULATION. Hemoglobin 25:3, pages 285-296.
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D. Filon, A. Oppenheim, E. A. Rachmilewitz, R. Kot & D. Ba Truc. (2000) Molecular Analysis of β-Thalassemia in Vietnam. Hemoglobin 24:2, pages 99-104.
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S. Agarwal, M. Pradhan, U. R. Gupta, S. Samai & S. S. Agarwal. (2000) Geographic and Ethnic Distribution of β-Thalassemia Mutations in Uttar Pradesh, India. Hemoglobin 24:2, pages 89-97.
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L. Varesi, G. Vona, M. Memmi, F. Marongiu & M. S. Ristaldi. (2000) β-Thalassemia Mutations in Corsica. Hemoglobin 24:3, pages 239-244.
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M. M. Marwan, C. A. Scerri, S. O. Zarroag, A. Cao, A. Kyrri, E. Kalogirou, M. Kleanthous, P. Ioannou, M. Angastiniotis & A. E. Felice. (1999) Comparative In Vivo Expression of β+-Thalassemia Alleles. Hemoglobin 23:3, pages 221-229.
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Articles from other publishers (38)
Chaima Abdelhafidh Sahli, Amina Bibi, Faida Ouali, Sondess Hadj Fredj, Boutheina Dakhlaoui, Rym Othmani, Naouel Laouini, Latifa Jouini, Fekria Ouenniche, Hajer Siala, Imed Touhami, Mariem Becher, Slaheddine Fattoum, Nour El Houda Toumi & Taieb Messaoud. (2013) Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia. Clinical Chemistry and Laboratory Medicine (CCLM) 51:11, pages 2115-2124.
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Chaima A. Sahli, Amina Bibi, Faida Ouali, Sondess Hadj Fredj, Boutheina Dakhlaoui, Rym Othmani, Naouel Laaouini, Latifa Jouini, Fekria Ouenniche, Hajer Siala, Imed Touhami, Mariem Becher, Slaheddine Fattoum, Nour El Houda Toumi & Taieb Messaoud. (2013) Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle cell disease and sickle cell thalassemia. Clinical Chemistry and Laboratory Medicine (CCLM) 51:8, pages 1595-1603.
Crossref
Crossref
A. El‐Beshlawy, A. El‐Shekha, M. Momtaz, F. Said, M. Hamdy, O. Osman, S. Meshaal, T. Gafaar & M. Petrou. (2012) Prenatal diagnosis for thalassaemia in Egypt: what changed parents' attitude?. Prenatal Diagnosis 32:8, pages 777-782.
Crossref
Crossref
Gururaj D. KulkarniSuyamindra S. KulkarniGurushantappa S. KadakolBhushan B. KulkarniPrakashgouda H. KyamangoudarBhaskar V.K.S. LakkakulaKumarasamy ThangarajTipperudra A. ShepurMuralidhar L. KulkarniPramod B. Gai. (2012) Molecular Basis of β-Thalassemia in Karnataka, India. Genetic Testing and Molecular Biomarkers 16:2, pages 138-141.
Crossref
Crossref
Muhammad UsmanMoinuddin MoinuddinSyed Azhar Ahmed. (2011) Role of iron deficiency anemia in the propagation of beta thalssemia gene. The Korean Journal of Hematology 46:1, pages 41.
Crossref
Crossref
Eunice Sindhuvi Edison, Ramachandran V. Shaji, Mammen Chandy & Alok Srivastava. (2011) Interaction of Hemoglobin E with Other Abnormal Hemoglobins. Acta Haematologica 126:4, pages 246-248.
Crossref
Crossref
Chia-Cheng Hung, Shee-Uan Chen, Shin-Yu Lin, Mei-Ya Fang, Li-Jung Chang, Yi-Yi Tsai, Li-Ting Lin, Yu-Shih Yang, Chien-Nan Lee & Yi-Ning Su. (2010) Preimplantation genetic diagnosis of β-thalassemia using real-time polymerase chain reaction with fluorescence resonance energy transfer hybridization probes. Analytical Biochemistry 400:1, pages 69-77.
Crossref
Crossref
Chia-Cheng Hung, Yi-Ning Su, Chia-Yun Lin, Yin-Fei Chang, Chien-Hui Chang, Wen-Fang Cheng, Chi-An Chen, Chien-Nan Lee & Win-Li Lin. (2008) Comparison of the mismatch-specific endonuclease method and denaturing high-performance liquid chromatography for the identification of HBB gene mutations. BMC Biotechnology 8:1.
Crossref
Crossref
Silvia Galbiati, Francesco Damin, Gabriele Di Carlo, Maurizio Ferrari, Laura Cremonesi & Marcella Chiari. (2008) Development of new substrates for high-sensitive genotyping of minority mutated alleles. ELECTROPHORESIS 29:23, pages 4714-4722.
Crossref
Crossref
Zosia B. Bornik & Hadi Dowlatabadi. (2008) Genomics in Cyprus: Challenging the social norms. Technology in Society 30:1, pages 84-93.
Crossref
Crossref
CHIA-CHENG HUNG, SHU-CHIN CHIEN, YI-NING SU, JIMMY PS CHERN, KAI-HSIN LIN & WIN-LI LIN. (2012) DENATURING HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY: AN EFFICIENT SCREENING APPROACH IN THE GENETIC DIAGNOSIS OF HEMOGLOBIN HAMMERSMITH. Biomedical Engineering: Applications, Basis and Communications 18:06, pages 343-347.
Crossref
Crossref
V. VIPRAKASIT, W. CHINCHANG, L. SUWANTHOL & V. S. TANPHAICHITR. (2005) Common origin of a rare beta-globin initiation codon mutation (ATGAGG) in Asians. Clinical and Laboratory Haematology 27:6, pages 409-415.
Crossref
Crossref
Worrawut Chinchang, Vip Viprakasit, Parichat Pung-Amritt, Voravarn S. Tanphaichitr & Pa-thai Yenchitsomanus. (2005) Molecular analysis of unknown β-globin gene mutations using polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) technique and its application in Thai families with β-thalassemias and β-globin variants. Clinical Biochemistry 38:11, pages 987-996.
Crossref
Crossref
Christopher T. Gordon, Vanessa J. Fox, Suzana Najdovska & Andrew C. Perkins. (2005) C/EBPδ and C/EBPγ bind the CCAAT-box in the human β-globin promoter and modulate the activity of the CACC-box binding protein, EKLF. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression 1729:1, pages 74-80.
Crossref
Crossref
Alessandra Falchi, Laurianne Giovannoni, Lucia Vacca, Veronica Latini, Giuseppe Vona & Laurent Varesi. (2005) ?-globin gene cluster haplotypes associated with ?-thalassemia on Corsica island. American Journal of Hematology 78:1, pages 27-32.
Crossref
Crossref
Maria De Angioletti, Giuseppina Lacerra, Leonilde Pagano, Mario Alessi, Rossana D'Avino, Laura Manca & Clementina Carestia. (2004)
β
-thalassaemia-87 C→G: relationship of the Hb F modulation and polymorphisms in compound heterozygous patients
. British Journal of Haematology 126:5, pages 743-749.
Crossref
Crossref
Roshan Colah, Anita Nadkarni, Ajit Gorakshakar, Supriya Phanasgaonkar, Reema Surve, P.G. Subramaniam, Nagnath Bondge, Kamala Pujari, Kanjaksha Ghosh & Dipika Mohanty. (2004) Impact of β globin gene mutations on the clinical phenotype of β thalassemia in India. Blood Cells, Molecules, and Diseases 33:2, pages 153-157.
Crossref
Crossref
Barbara Foglieni, Laura Cremonesi, Maurizio Travi, Anna Ravani, Antonino Giambona, Maria Cristina Rosatelli, Chiara Perra, Paolo Fortina & Maurizio Ferrari. (2004) β-Thalassemia Microelectronic Chip: A Fast and Accurate Method for Mutation Detection. Clinical Chemistry 50:1, pages 73-79.
Crossref
Crossref
Maria De Angioletti, Giuseppina Lacerra, Vincenzo Sabato & Clementina Carestia. (2004) β+45 G → C: a novel silent β-thalassaemia mutation, the first in the Kozak sequence. British Journal of Haematology 124:2, pages 224-231.
Crossref
Crossref
Anju Gupta, Yukio Hattori, Usha R. Gupta, Swati Sarwai, Nitu Nigam, Pragya Singhal & Sarita Agarwal. (2003) Molecular Genetic Testing of β-Thalassemia Patients of Indian Origin and a Novel 8-bp Deletion Mutation at Codons 36/37/38/39. Genetic Testing 7:2, pages 163-168.
Crossref
Crossref
Ramachandran V Shaji, Eunice Sindhuvi Edison, Balasubramanian Poonkuzhali, Alok Srivastava & Mammen Chandy. (2003) Rapid Detection of β-Globin Gene Mutations and Polymorphisms by Temporal Temperature Gradient Gel Electrophoresis. Clinical Chemistry 49:5, pages 777-781.
Crossref
Crossref
Maurizio Ferrari, Stefania Stenirri, Pierangelo Bonini & Laura Cremonesi. (2003) Molecular Diagnostics by Microelectronic Microchips. Clinical Chemistry and Laboratory Medicine 41:4.
Crossref
Crossref
Rosa Santacroce, Antonia Ratti, Francesco Caroli, Barbara Foglieni, Alessandro Ferraris, Laura Cremonesi, Maurizio Margaglione, Marco Seri, Roberto Ravazzolo, Gabriella Restagno, Bruno Dallapiccola, Eric Rappaport, Eleanor S Pollak, Saul Surrey, Maurizio Ferrari & Paolo Fortina. (2002) Analysis of Clinically Relevant Single-Nucleotide Polymorphisms by Use of Microelectronic Array Technology. Clinical Chemistry 48:12, pages 2124-2130.
Crossref
Crossref
Maria De Angioletti, Giuseppina Lacerra, Carlo Gaudiano, Gabriella Mastrolonardo, Leonilde Pagano, Lucia Mastrullo, Santa Masciandaro & Clementina Carestia. (2002) Epidemiology of the delta globin alleles in southern Italy shows complex molecular, genetic, and phenotypic features. Human Mutation 20:5, pages 358-367.
Crossref
Crossref
Anju Gupta, Yukio Hattori & Sarita Agarwal. (2002) Initiation codon mutation in an Asian Indian family. American Journal of Hematology 71:2, pages 134-136.
Crossref
Crossref
Paula Faustino, Ana Batalha Reis, Helena Feliciano, Lénia Ferrão, Patrícia Pereira, Isabel Picanço, Armandina Miranda, Teresa Seixas, Luísa Romão, Esmeraldina Correia Júnior & João Lavinha. (2002)
Asymptomatic homozygous deletional β
0
‐thalassemia in an African individual
. American Journal of Hematology 70:3, pages 232-236.
Crossref
Crossref
Antonio Cao, Maria Cristina Rosatelli, Giovanni Monni & Renzo Galanello. (2002) Screening for thalassemia. Obstetrics and Gynecology Clinics of North America 29:2, pages 305-328.
Crossref
Crossref
Antonio Cao. (2002) Carrier screening and genetic counselling in β-thalassemia. International Journal of Hematology 76:S2, pages 105-113.
Crossref
Crossref
Deborah Rund & Eliezer Rachmilewitz. (2001) Pathophysiology of α- and β-thalassemia: Therapeutic implications. Seminars in Hematology 38:4, pages 343-349.
Crossref
Crossref
Adriana Muñiz, Gisela Martinez, João Lavinha & Paula Pacheco. (2000) β-Thalassaemia in Cubans: Novel allele increases the genetic diversity at theHBB locus in the Caribbean. American Journal of Hematology 64:1, pages 7-14.
Crossref
Crossref
S Agarwal, Y Hattori & Ss Agarwal. (2001) Identification of a novel frameshift β‐thalassemia mutation in an Asian Indian. Clinical Genetics 57:4, pages 311-312.
Crossref
Crossref
Chitra Thakur (Mahadik)Flavian Vaz, Monisha Banerjee, Chhaya Kapadia, P. G. Natrajan, Harsha Yagnik & Sudha Gangal. (2000) Prenatal diagnosis of ?-thalassaemia and other haemoglobinopathies in India. Prenatal Diagnosis 20:3, pages 194-201.
Crossref
Crossref
Antonio Cao & Paolo Moi. (2000) Genetic Modifying Factors in β-Thalassemia. cclm 38:2, pages 123-132.
Crossref
Crossref
E. Maragoudaki, E. Kanavakis, J. Traeger‐Synodinos, C. Vrettou, M. Tzetis, A. Metaxotou‐Mavrommati & C. Kattamis. (2002) Molecular, haematological and clinical studies of the −101 C → T substitution of the β‐globin gene promoter in 25 β‐thalassaemia intermedia patients and 45 heterozygotes. British Journal of Haematology 107:4, pages 699-706.
Crossref
Crossref
Roshan Colah & Dipika Mohanty. (1998) β-Thalassemias : Expression, molecular mechanisms and mutations in Indians. The Indian Journal of Pediatrics 65:6, pages 815-823.
Crossref
Crossref
Luis A. Ugozzoli, J. D. Lowery, A. A. Reyes, C.-I. P. Lin, A. Re, F. Locati, R. Galanello, L. Macioni, A. Maggio, A. Giambona, A. Loutradi, M. Boussiou & R. Bruce Wallace. (1998) Evaluation of the BeTha Gene 1 Kit for the Qualitative Detection of the Eight Most Common Mediterranean β-Thalassemia Mutations. American Journal of Hematology 59:3, pages 214-222.
Crossref
Crossref
Maragoudaki, Vrettou, Kanavakis, Traeger‐Synodinos, Metaxotou‐Mavrommati & Kattamis. (2002) Molecular, haematological and clinical studies of a silent β‐gene C → G mutation at 6 bp 3′ to the termination codon (+1480 C → G) in twelve Greek families. British Journal of Haematology 103:1, pages 45-51.
Crossref
Crossref
Antonio Cao, Renzo Galanello & M. Cristina Rosatelli. (1998) 8 Prenatal diagnosis and screening of the haemoglobinopathies. Baillière's Clinical Haematology 11:1, pages 215-238.
Crossref
Crossref