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Hemoglobin
international journal for hemoglobin research
Volume 23, 1999 - Issue 2
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BriefNote Article

Hb siriraj: A G→A substitution at codon 7 of the β-globin chain creates an Mboll cutting site

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Pages 197-199 | Received 19 Nov 1998, Accepted 14 Dec 1998, Published online: 05 Aug 2009

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Read on this site (10)

Zhi-Yang Guan, Ze-Yan Zhong, Zhi-Bang Xu, Jian-Hong Chen & Yan-Hui Liu. (2022) A Case of Misdiagnosis Caused by the Coinheritance of Hb G-Siriraj [β7(A4)Glu→Lys; HBB: c.22G>A] and Hb H Disease. Hemoglobin 46:6, pages 338-340.
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Su-Ching Liu, Ching-Tien Peng, Tsai-Hsiu Lin, Shiow-Jain Wang, Mu-Chin Shih, Ni Tien, Chao-Chin Chang, Jang-Jih Lu & Chien-Yu Lin. (2011) Molecular Lesion Frequency Of Hemoglobin Gene Disorders In Taiwan. Hemoglobin 35:3, pages 228-236.
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Hung-Chang Shih, Mu-Chin Shih, Yu-Chang Chang, Ching-Tien Peng, Tien-Jye Chang & Jan-Gowth Chang. (2007) Hb Hekinan in a Taiwanese Subject: A G→T Substitution at Codon 27 of the α1-Globin Gene Abolishes an HaeIII Site. Hemoglobin 31:4, pages 495-498.
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Mu-Chin Shih, Kang-His Wu, Su-Ching Liu & Jan-Gowth Chang. (2005) Hb Tak: A β Chain Elongation at the End of the β Chain, in a Taiwanese. Hemoglobin 29:1, pages 65-67.
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Mu‐Chin Shih, Ching‐Tien Peng, Jan‐Yi Chang, Su‐Ching Liu, Pao‐Lin Kuo & Jan‐Gowth Chang. (2003) Hb Prato [α31(B12)Arg→Ser (α2)] and α‐Thalassemia in a Taiwanese. Hemoglobin 27:1, pages 45-47.
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Mu‐Chin Shih, Ching‐Tien Peng & Jan‐Gowth Chang. (2003) Association of Hb G‐Chinese [α30(B11)Glu→Gln] with α‐Thalassemia‐1 of the Thai Type in a Taiwanese Family. Hemoglobin 27:1, pages 41-44.
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Jan-Gowth Chang, Mu-Chin Shih, Su-Ching Liu, Chih-Mei Chen, Wen-Ling Chan, Tai-Ping Lee & Ching-Tien Peng. (2002) Hb G-HONOLULU [α30(B11)Glu→Gln (α2)], Hb J-MEINUNG [β56(D7)Gly→Asp], AND β-THALASSEMIA [CODONS 41/42 (—TCTT)] IN A TAIWANESE FAMILY. Hemoglobin 26:3, pages 325-328.
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Jan-Gowth Chang, Mu-Chin Shih, Su-Ching Liu, Chih-Mei Chen, Wen-Ling Chan & Ching-Tien Peng. (2002) Hb G-CHINESE: A G → C SUBSTITUTION AT CODON 30 OF THE α2-GLOBIN GENE CREATES A PstI CUTTING SITE. Hemoglobin 26:1, pages 95-97.
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Jan-Gowth Chang, Hsi-Che Liu, Mu-Chin Shih, Su-Ching Liu, Wen-Ling Chan & Fuu-Jen Tsai. (2002) UNSTABLE Hb PERTH IN A TAIWANESE SUBJECT: A T → C SUBSTITUTION AT CODON 32 OF THE β-GLOBIN GENE CREATES AN MspI SITE. Hemoglobin 26:1, pages 91-94.
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Jan-Gowth Chang, Mu-Chin Shih, Su-Ching Liu, Wen-Ling Chan & Ching-Tien Peng. (2001) Hb MANITOBA IN A TAIWANESE FAMILY: A C → A SUBSTITUTION AT CODON 102 OF THE α2-GLOBIN GENE. Hemoglobin 25:4, pages 437-439.
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Articles from other publishers (3)

Hui-Ching Wang, Li-Ling Hsieh, Yi-Chang Liu, Hui-Hua Hsiao, Shu-Kai Lin, Wen-Chan Tsai & Ta-Chih Liu. (2016) The epidemiologic transition of thalassemia and associated hemoglobinopathies in southern Taiwan. Annals of Hematology 96:2, pages 183-188.
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Ching-Tien Peng, Su-Ching Liu, Yi-Chin Peng, Tsai-Hsiu Lin, Shiow-Jain Wang, Ching-Yi Le, Mu-Chin Shih, Ni Tien, Jang-Jih Lu & Chien-Yu Lin. (2013) Distribution of thalassemias and associated hemoglobinopathies identified by prenatal diagnosis in Taiwan. Blood Cells, Molecules, and Diseases 51:3, pages 138-141.
Crossref
H.-J. LIN, M.-C. SHIH, C.-T. PENG, T.-C. LIU, K.-W. CHEN, H.-C. SHIH & J.-G. CHANG. (2010) Hematological features and molecular lesions of hemoglobin gene disorders in Taiwanese patients. International Journal of Laboratory Hematology 32:1p2, pages 1-7.
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