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Hemoglobin
international journal for hemoglobin research
Volume 39, 2015 - Issue 3
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Short Communication

Hb H Hydrops Fetalis Syndrome Caused by Association of the − −SEA Deletion and Hb Constant Spring (HBA2: c.427T > C) Mutation in a Chinese Family

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Pages 216-219 | Received 29 Jul 2014, Accepted 15 Oct 2014, Published online: 21 Apr 2015

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Hai-Shen Tang, Yi Xiong & Dong-Zhi Li. (2023) Fetal Hemoglobin H Hydrops Fetalis: Another Three Case Reports. Hemoglobin 47:2, pages 102-104.
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Phongsathorn Wichian, Supawadee Yamsri, Attawut Chaibunruang, Cholthicha KerdKaew, Dhanawan Thongsee, Hataichanok Srivorakun & Supan Fucharoen. (2021) Direct PCR assays without DNA extraction for rapid detection of hemoglobin Constant Spring and Pakse' genes: application for carrier screening and prenatal diagnosis. Scandinavian Journal of Clinical and Laboratory Investigation 81:7, pages 557-563.
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Fan Jiang, Li-Li Xu, Gui-Lan Chen, Jian-Ying Zhou, Jian Li, Xue-Wei Tang, Lian-Dong Zuo & Dong-Zhi Li. (2020) Hematological Characteristics of Hb Constant Spring (HBA2: c.427T>C) Carriers in Mainland China. Hemoglobin 44:2, pages 86-88.
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Qiang Li, Yihong Li, Mei Zhong, Victor Wei Zhang, Wangjie Jin, Shaoyuan Li & Liyan Li. (2018) A Rare Hb H Hydrops Fetalis Syndrome Caused by the – –SEA Deletion in Combination with the Rare Hb Hirosaki Mutation in a Chinese Patient. Hemoglobin 42:4, pages 278-280.
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Articles from other publishers (9)

Sitthichai Panyasai, Surada Satthakarn & Amphai Phasit. (2023) Effective screening of hemoglobin Constant Spring and hemoglobin Paksé with several forms of α- and β-thalassemia in an area with a high prevalence and heterogeneity of thalassemia using capillary electrophoresis. Heliyon 9:8, pages e19116.
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Duantida Songdej, Manunya Tandhansakul, Pakawan Wongwerawattanakoon, Nongnuch Sirachainan, Pimlak Charoenkwan & Ampaiwan Chuansumrit. (2023) Severity scoring system to guide transfusion management in pediatric non‐deletional HbH. Pediatrics International 65:1.
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Duantida Songdej & Suthat Fucharoen. (2022) Alpha-Thalassemia: Diversity of Clinical Phenotypes and Update on the Treatment. Thalassemia Reports 12:4, pages 157-172.
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Հ․ Ա. Գրիգորյան, Լ․ Ս․ Հակոբյան, Լ. Մ. Քրմոյան, Ս․ Հ․ Դանելյան & Լ․ Հ․ Վաղարշակյան. (2022) Թալասեմիաների ընդհանուր բնութագիրը. Medical Science of Armenia, pages 20-30.
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Suchaya Luewan, Pimlak Charoenkwan, Supatra Sirichotiyakul & Theera Tongsong. (2020) Fetal haemoglobin H‐Constant Spring disease: a role for intrauterine management. British Journal of Haematology 190:4.
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Patcharee Komvilaisak, Ratana Komvilaisak, Arunee Jetsrisuparb, Surapon Wiangnon, Junya Jirapradittha, Pakaphan Kiatchoosakun & Goonapa Fucharoen. (2018) Fetal Anemia Causing Hydrops Fetalis From an Alpha-Globin Variant: Homozygous Hemoglobin Constant Spring. Journal of Pediatric Hematology/Oncology 40:5, pages 405-408.
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Vip Viprakasit & Supachai Ekwattanakit. (2018) Clinical Classification, Screening and Diagnosis for Thalassemia. Hematology/Oncology Clinics of North America 32:2, pages 193-211.
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Chi-Kong Li. (2017) New trend in the epidemiology of thalassaemia. Best Practice & Research Clinical Obstetrics & Gynaecology 39, pages 16-26.
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Annemarie DeLeo & Sadie Geraghty. (2016) Thalassaemia in pregnancy: Contemporary care for a timeless disease. British Journal of Midwifery 24:8, pages 567-572.
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