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Hemoglobin
international journal for hemoglobin research
Volume 25, 2001 - Issue 1
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A KOREAN FAMILY WITH A DOMINANTLY INHERITED β-THALASSEMIA DUE TO Hb DURHAM-N.C./BRESCIA [β114(G16)Leu→Pro]

Ji Yeon Kim Department of Clinical Pathology, Seoul National University College of Medicine, Seoul, 110-744, Korea
,
Sung Sup Park Department of Clinical Pathology, Seoul National University College of Medicine, Seoul, 110-744, Korea; Department of Clinical Pathology, Seoul National University Hospital, 28 Yongon-dong, Chongno-gu, Seoul, 110-744, Korea
,
Sung Hyun Yang Department of Internal Medicine, Dankook University Hospital, Cheonan, 330-715, Korea
,
Se-Ick Joo Department of Clinical Pathology, Seoul National University College of Medicine, Seoul, 110-744, Korea
,
Young Joon Lee Department of Clinical Pathology, Seoul National University College of Medicine, Seoul, 110-744, Korea
,
Eun Kyung Ra Department of Clinical Pathology, Seoul National University College of Medicine, Seoul, 110-744, Korea
,
Sue Shin Department of Clinical Pathology, Seoul National University College of Medicine, Seoul, 110-744, Korea
,
Eui Chong Kim Department of Clinical Pathology, Seoul National University College of Medicine, Seoul, 110-744, Korea
&
Han-Ik Cho Department of Clinical Pathology, Seoul National University College of Medicine, Seoul, 110-744, Korea
 show all
Pages 79-89 | Received 04 Apr 2000, Accepted 10 Aug 2000, Published online: 07 Jul 2009

Citations (7)

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Xiao-Mei Lin, Fan Jiang, Jian Li & Dong-Zhi Li. (2022) Dominantly Inherited β-Thalassemia Caused by a Single Nucleotide Deletion in Exon 3 of the β-Globin Gene: Hb Xiangyang (HBB: c.393delT). Hemoglobin 46:4, pages 253-255.
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Monica Cannata, Filippo Cassarà, Margherita Vinciguerra, Paola Licari, Cristina Passarello, Filippo Leto, Carmen Lo Pinto, Lorella Pitrolo, Riccardo Ganci, Aurelio Maggio & Antonino Giambona. (2019) Double Heterozygosity for Hb Durham-N.C. (HBB: c.344T>C) [β114(G16)Leu→Pro] and the IVS-I-110 (HBB: c.93-21G>A) Causing a Severe β-Thalassemia Phenotype. Hemoglobin 43:3, pages 210-213.
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Joanne Traeger-Synodinos & Cornelis L. Harteveld. (2017) Preconception carrier screening and prenatal diagnosis in thalassemia and hemoglobinopathies: challenges and future perspectives. Expert Review of Molecular Diagnostics 17:3, pages 281-291.
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Samaneh Farashi, Fariba Rad, Bahram Shahmohammadi, Hashem Imanian, Azita Azarkeivan & Hossein Najmabadi. (2016) First Report of a Dominantly Inherited β-Thalassemia Caused by a Novel Elongated β-Globin Chain. Hemoglobin 40:2, pages 102-107.
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Sung Sup Park, Young Joon Lee, Ji Yeon Kim, Sae Ick Joo, Yukio Hattori, Yuzo Ohba & Han-Ik Cho. (2002) β-THALASSEMIA IN THE KOREAN POPULATION. Hemoglobin 26:2, pages 135-145.
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Articles from other publishers (2)

Irene Jo, Woori Jang, Hyojin Chae, So-Young Kim, Myungshin Kim, Yonggoo Kim & Kyungja Han. (2017) Hemoglobin Kansas: First Korean Family and Literature Review. Annals of Laboratory Medicine 37:4, pages 352-354.
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Sung Sup Park & Han-Ik Cho. (2002) β-Thalassemia in the Korean population. International Journal of Hematology 76:S2, pages 93-95.
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