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Hemoglobin
international journal for hemoglobin research
Volume 35, 2011 - Issue 4
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Original Article

β-Thalassemia Mutations Found During 1 Year of Prenatal Diagnoses in Fars Province, Iran

Mohammad Saeid RahiminejadDivision of Pediatric Hematology Oncology, Children’s Medical Center, Tehran University of Medical Sciences (TUMS), Tehran, IranCorrespondence[email protected]
,
Sirous ZeinaliGenetic Laboratory and Research Center, Pasteur Institute, Tehran, Iran
,
Abdolreza AfrasiabiGenetic Laboratory and Research Center, Shahid Dastgheib Hospital, Shiraz University of Medical Sciences, Shiraz, Iran
&
Ali Kord ValeshabadStudents’ Scientific Research Center (SSRC), Tehran University of Medical Sciences (TUMS), Tehran, Iran;Farzan Clinical Research Institute, Tehran, Iran
Pages 331-337 | Received 27 Dec 2010, Accepted 09 May 2010, Published online: 28 Jul 2011

Citations (4)

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Read on this site (2)

Mina Ebrahimi, Javad Mohammadi-Asl & Fakher Rahim. (2021) The worldwide molecular spectrum and distribution of thalassaemia: a systematic review. Annals of Human Biology 48:4, pages 307-312.
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Hossam Murad, Faten Moassas, Rami Jarjour, Yasser Mukhalalaty & Walid Al-Achkar. (2014) Prenatal Molecular Diagnosis of β-Thalassemia and Sickle Cell Anemia in the Syrian Population. Hemoglobin 38:6, pages 390-393.
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Articles from other publishers (2)

Mina Ebrahimi, Javad Mohammadi-asl & Fakher Rahim. (2020) Molecular spectrum and distribution of hemoglobinopathies in southwest of Iran: a seven-year retrospective study. Journal of Hematopathology 13:2, pages 97-103.
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Nejat Mahdieh & Bahareh Rabbani. (2016) Beta thalassemia in 31,734 cases with HBB gene mutations: Pathogenic and structural analysis of the common mutations; Iran as the crossroads of the Middle East. Blood Reviews 30:6, pages 493-508.
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