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Hemoglobin
international journal for hemoglobin research
Volume 22, 1998 - Issue 5-6
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Original Article

Molecular Diagnosis and Characterization of Hb Zürich [β63(E7)His→Arg] Carriers in a Kentucky Family

M. D. P. Aguinaga Comprehensive Sickle Cell Center; Department of Obstetrics and Gynecology, Meharry Medical College, Nashville, TN, 37208, USA
,
C. J. Wright Comprehensive Sickle Cell Center; Department of Biology, Western Kentucky University Bawling Green, KY, 42101, USA
,
P. D. Roa Comprehensive Sickle Cell Center; Department of Pediatrics, Meharry Medical College, Nashville, TN, 37208, USA
,
F. Terrell Comprehensive Sickle Cell Center
,
E. A. Turner Comprehensive Sickle Cell Center; Department of Pediatrics, Meharry Medical College, Nashville, TN, 37208, USA
&
M. Houston Comprehensive Sickle Cell Center; Department of Biology, Western Kentucky University Bawling Green, KY, 42101, USA
Pages 509-515 | Received 05 Feb 1998, Accepted 07 Jul 1998, Published online: 07 Jul 2009

Citations (3)

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Read on this site (1)

M. D. P. Aguinaga, F. Kutlar, E. A. Turner & D. Park. (2000) HB Inkster [α85(F6)ASP→VAL] Found in a Caucasian male with Polycythemia. Hemoglobin 24:4, pages 333-339.
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Articles from other publishers (2)

Carol L.S. Yan, Nelson C. N. Chan, Grace K. S. Lam, Ka Y. Ng, Chi K. Cheng & Chi‐Kong Li. (2019) A new form of thalassemia intermedia: Compound heterozygous beta thalassemia and hemoglobin Zurich. Pediatric Blood & Cancer 66:6, pages e27720.
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Xiu-Yun Yao, Jie Yu, Shi-Ping Chen, Jian-Wen Xiao, Qi-Chen Zheng, Hai-Yan Liu, Lei Zhang, Ying Xian & Lin Zou. (2013) Prevalence and genetic analysis of α-thalassemia and β-thalassemia in Chongqing area of China. Gene 532:1, pages 127-131.
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