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Hemoglobin
international journal for hemoglobin research
Volume 13, 1989 - Issue 4
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Original Article

Hemoglobin Hekinan [α227(B8)Glu→Aspβ2] Detected in Guyana

G. Merault INSERM U.91 Centre Hospitalier Regional et Universitaire, 97159 Pointe-à-Pitre, Guadeloupe, French West Indies
,
L. Keclard INSERM U.91 Centre Hospitalier Regional et Universitaire, 97159 Pointe-à-Pitre, Guadeloupe, French West Indies
,
L. Desfontaines INSERM U.91 Centre Hospitalier Regional et Universitaire, 97159 Pointe-à-Pitre, Guadeloupe, French West Indies
,
C. Saint-Matin INSERM U.91 Centre Hospitalier Regional et Universitaire, 97159 Pointe-à-Pitre, Guadeloupe, French West Indies
,
Y. Blouquit INSERM U.91 Hôpital Henri Mondor, 94010, Créteil, France
,
J. Rosa INSERM U.91 Hôpital Henri Mondor, 94010, Créteil, France
&
F. Galacteros INSERM U.91 Hôpital Henri Mondor, 94010, Créteil, France
 show all
Pages 397-402 | Received 01 Feb 1988, Accepted 08 Feb 1989, Published online: 07 Jul 2009

Citations (8)

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Read on this site (4)

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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Lukana Ngiwsara, Chantragan Srisomsap, Pranee Winichagoon, Suthat Fucharoen & Jisnuson Svasti. (2004) Two Cases of Compound Heterozygosity for Hb Hekinan [α27(B8)Glu→Asp (α1)] and α‐Thalassemia in Thailand. Hemoglobin 28:2, pages 145-150.
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M. L. Ribeiro & G. P. Tamagnini. (1997) Hemoglobin Disorders in Macao. Hemoglobin 21:3, pages 271-279.
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W. Zhao, J. B. Wilson, B. B. Webber, A. Kutlar, G. P. Tamagnini, B. Kuan & T. H. J. Huisnan. (1990) Hb Hekinan Observed in Three Chinese from Macau; Identification of the Gag→Gat Mutation in the αl-Globin Gene. Hemoglobin 14:6, pages 627-635.
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Articles from other publishers (4)

Giuseppina Barberio, Massimo Mogni, Massimo Maffei, Giovanni Ivaldi & Livio Caberlotto. (2018) Appropriatezza dei percorsi diagnostici per le emoglobinopatie: il caso Hb HekinanDiagnostic appropriateness of the pathways for hemoglobinopathies: the example of Hb Hekinan. La Rivista Italiana della Medicina di Laboratorio - Italian Journal of Laboratory Medicine 14:1, pages 50-53.
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Kamran Moradkhani, Claude Préhu, John Old, Shirley Henderson, Vera Balamitsa, Hong-Yuan Luo, Man-Chiu Poon, David H. K. Chui, Henri Wajcman & George P. Patrinos. (2008) Mutations in the paralogous human α-globin genes yielding identical hemoglobin variants. Annals of Hematology 88:6, pages 535-543.
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S. Chunpanich, K. Ayukarn, K. Sanchaisuriya, G. Fucharoen & S. Fucharoen. (2004) Laboratory diagnosis of a compound heterozygosity for Hb Hekinan [alpha27(B8) Glu-Asp] and a deletional alpha-thalassaemia 2 in Thailand. Clinical and Laboratory Haematology 26:5, pages 355-358.
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Supan Fucharoen, Yossombat Changtrakun, Thawalwong Ratanasiri, Goonnapa Fucharoen & Kanokwan Sanchaisuriya. (2003) Complex interaction of Hb Hekinan [α27(B8) Glu-Asp] and Hb E [β26(B8) Glu-Lys] with a deletional α-thalassemia 1 in a Thai family. European Journal of Haematology 70:5, pages 304-309.
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