Citations (34)
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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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Hajar Eftekhari, Ahmad Tamaddoni, Hassan Mahmoudi Nesheli, Mohsen Vakili, Sadegh Sedaghat, Ali Banihashemi, Mandana Azizi, Reza Youssefi Kamangar & Haleh Akhavan-Niaki. (2017) A Comprehensive Molecular Investigation of α-Thalassemia in an Iranian Cohort from Different Provinces of North Iran. Hemoglobin 41:1, pages 32-37.
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Rawand P. Shamoon, Nasir A. S. Al-Allawi, Maria D. Cappellini, Elena Di Pierro, Valentina Brancaleoni & Francesca Granata. (2015) Molecular Basis of β-Thalassemia Intermedia in Erbil Province of Iraqi Kurdistan. Hemoglobin 39:3, pages 178-183.
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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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Huseyin Gulen, Ozlem Hanimeli, Ozlem Karaca & Fatma Taneli. (2012) α-Thalassemia Frequency and Mutations in Children with Hypochromic Microcytic Anemias and Relation with β-Thalassemia, Iron Deficiency Anemia. Pediatric Hematology and Oncology 29:3, pages 241-246.
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Nasrollah Saleh-Gohari & Arezo Khosravi-Mashizi. (2010) Spectrum of α-Globin Gene Mutations in the Kerman Province of Iran. Hemoglobin 34:5, pages 451-460.
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Nasir A.S. Al-Allawi, Ameer I.A. Badi, Hasham Imanian, Nooshin Nikzat, Jaladet M.S. Jubrael & Hossein Najmabadi. (2009) Molecular Characterization of α-Thalassemia in the Dohuk Region of Iraq. Hemoglobin 33:1, pages 37-44.
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Mehmet Akif Çürük. (2007) Hb H (β4) Disease in Çukurova, Southern Turkey. Hemoglobin 31:2, pages 265-271.
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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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Amine Zorai, Salem Abbes, Claude Préhu, Souheil Omar, Nathalie Gerard, Raouf Hafsia, Bouaziz Asma, Fethi Guemira & Kousay Dellagi. (2003) Hb H Disease Among Tunisians: Molecular Characterization of α‐Thalassemia Determinants and Hematological Findings. Hemoglobin 27:1, pages 57-61.
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Vichai Laosombat, Supan Fucharoen & Aranya Wiriyasateinkul. (2001) INTERACTION OF THE α2 POLYADENYLATION SIGNAL MUTATION (AATAAA → AATA– –) AND α0-THALASSEMIA (– –SEA), RESULTING IN Hb H DISEASE IN A THAI PATIENT. Hemoglobin 25:4, pages 383-389.
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M. Akif Çürük, Yurdanur Kilinç, Cüneyt Evrüke, Fatma T. Ozgünen, Kýymet Aksoy & Guneş T. Yüreğir. (2001) PRENATAL DIAGNOSIS OF Hb H DISEASE CAUSED BY A HOMOZYGOSITY FOR THEα2 POLY A (AATAAA→ AATAAG) MUTATION. Hemoglobin 25:2, pages 255-258.
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C. Öner, R. Öner, E. Birben, H. Balkan, F. Giümrük, A. Gürgey & L. Altay. (1998) Short Communication: HB H Disease with Homozygosity for Red Cell G6PD Deficiency in a Turkish Female. Hemoglobin 22:2, pages 157-160.
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Articles from other publishers (21)
Yusuf DÖĞÜŞ, Petek ÇÜRÜK & Akif ÇÜRÜK. (2023) Is genetic counseling important in hemoglobin H disease?Hemoglobin H hastalığında genetik danışmanlık önemli midir?. Cukurova Medical Journal 48:2, pages 723-727.
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Mohammad Hamid, Bijan keikhaei, Hamid Galehdari, Alihossein Saberi, Alireza Sedaghat, Gholamreza Shariati & Marziye Mohammadi-Anaei. (2022) Genotype–phenotype correlation in patients with deletional and nondeletional mutations of Hb H disease in Southwest of Iran. Scientific Reports 12:1.
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Selahaddin Tekeş, Diclehan Oral, Murat Söker, Selda Şimşek, Veysiye Hülya Uzel & Mehmet Akif Çürük. (2022) Analysis of beta globin gene mutations in Diyarbakir. Turkish Journal of Biochemistry 47:1, pages 113-118.
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Mostafa Paridar, Ebrahim Azizi, Bijan Keikhaei, Vahideh Takhviji, Iman Baluchi & Abbas Khosravi. (2019) Iranian patients with hemoglobin H disease: genotype–phenotype correlation. Molecular Biology Reports 46:5, pages 5041-5048.
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Oded Gilad, Orna Steinberg Shemer, Orly Dgany, Tanya Krasnov, Michal Nevo, Sharon Noy-Lotan, Ron Rabinowicz, Nofar Amitai, Shifra Ben-Dor, Isaac Yaniv, Joanne Yacobovich & Hannah Tamary. (2017) Molecular diagnosis of α-thalassemia in a multiethnic population. European Journal of Haematology 98:6, pages 553-562.
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Ahmet Genç, Yusuf Sevgiler, Süleyman Bayram & Eyyüp Rencüzoğulları. (2016) The prevalence and genotypes of alpha-thalassemia in Adıyaman: two rare alpha variants. Turkish Journal of Biochemistry 41:6, pages 467-472.
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Samaneh Farashi & Hossein Najmabadi. (2015) Diagnostic pitfalls of less well recognized HbH disease. Blood Cells, Molecules, and Diseases 55:4, pages 387-395.
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Hüseyin Onay, Ayça Aykut, Emin Karaca, Asude Durmaz, Aslı Ece Solmaz, Özgür Çoğulu, Yeşim Aydınok, Canan Vergin & Ferda Özkınay. (2015) Molecular spectrum of α-globin gene mutations in the Aegean region of Turkey: first observation of three α-globin gene mutations in the Turkish population. International Journal of Hematology 102:1, pages 1-6.
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Sevcan Tug Bozdogan, Ozge Ozalp Yuregir, Nurhilal Buyukkurt, Huseyin Aslan, Zeynep Canan Ozdemir & Tomasz Gambin. (2014) Alpha-Thalassemia Mutations in Adana Province, Southern Turkey: Genotype-Phenotype Correlation. Indian Journal of Hematology and Blood Transfusion 31:2, pages 223-228.
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Chantal Farra, Rebecca Badra, Farah Fares, Samar Muwakkit, Ghassan Dbaibo, Ibrahim Dabbous, Hanine Ashkar, Carla Mounsef & Miguel R. Abboud. (2015) Alpha thalassemia allelic frequency in Lebanon. Pediatric Blood & Cancer 62:1, pages 120-122.
Crossref
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Muhammet Murat Celik, Ramazan Gunesacar, Gonul Oktay, Gulay Gulbol Duran & Hasan Kaya. (2013) Spectrum of α-thalassemia mutations including first observation of - -FIL deletion in Hatay Province, Turkey. Blood Cells, Molecules, and Diseases 51:1, pages 27-30.
Crossref
Crossref
Recep Sütçü, Firdevs Aylak, Havva Koçak, Tansu Sipahi, Hüseyin Vural & Namık Delibaş. (2011) The investigation of distribution of hereditary alpha-thalassemia mutations in Isparta reservoir. European Journal of Basic Medical Sciences 1:1, pages 28-32.
Crossref
Crossref
Dilay Ciglidag Dungul, Hilal Ozdag & Nejat Akar. (2011) Hemoglobin alpha 2 gene +861 G>A polymorphism in Turkish population. Egyptian Journal of Medical Human Genetics 12:1, pages 59-62.
Crossref
Crossref
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallDouglas R. Higgs. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin
266
295
.
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallDouglas R. Higgs. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin
239
240
.
Ali HellaniElias FadelShaker El-SadadiHamdan El-SweilamAhmed El-DawoodKhaled K. Abu-Amero. (2009) Molecular Spectrum of α-Thalassemia Mutations in Microcytic Hypochromic Anemia Patients from Saudi Arabia. Genetic Testing and Molecular Biomarkers 13:2, pages 219-221.
Crossref
Crossref
Helene Puehringer, Hossein Najmabadi, Hai-Yang Law, Walter Krugluger, Vip Viprakasit, Serge Pissard, Erol Baysal, Ali Taher, Chantal Farra, Amein Al-Ali, Suad Al-Ateeq & Christian Oberkanins. (2007) Validation of a reverse-hybridization StripAssay for the simultaneous analysis of common α-thalassemia point mutations and deletions. Clinical Chemical Laboratory Medicine 45:5.
Crossref
Crossref
David H. K. ChuiSuthat FucharoenVivian Chan. (2003) Hemoglobin H disease: not necessarily a benign disorder. Blood 101:3, pages 791-800.
Crossref
Crossref
John S. Waye, Barry Eng, Margaret Patterson, Lynda Walker, Manuel D. Carcao, Nancy F. Olivieri & David H.K. Chui. (2001) Hemoglobin H (Hb H) disease in Canada: Molecular diagnosis and review of 116 cases. American Journal of Hematology 68:1, pages 11-15.
Crossref
Crossref
D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes
733
821
.
Varda Oron-Karni, Dvora Filon, Yulia Shifrin, Elchanan Fried, Galina Pogrebijsky, Ariella Oppenheim & Deborah Rund. (2000) Diversity of ?-globin mutations and clinical presentation of ?-thalassemia in Israel. American Journal of Hematology 65:3, pages 196-203.
Crossref
Crossref