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Hemoglobin
international journal for hemoglobin research
Volume 1, 1976 - Issue 1
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Original Article

Hemoglobin Riyadh-α2β2 (120 [GH3] Lys→Asn): A New Variant Found in Association with α-Thalassemia and Iron Deficiency

M. A. F. El-Hazmi University Department of Clinical Biochemistry, (W.H.O. Collaborating Center for Abnormal Hemoglobins) Addenbrooke's Hospital, Cambridge, England
&
H. Lehmann University Department of Clinical Biochemistry, (W.H.O. Collaborating Center for Abnormal Hemoglobins) Addenbrooke's Hospital, Cambridge, England
Pages 59-74 | Published online: 07 Jul 2009

Citations (31)

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M. F. H. Carver & T. H. J. Huisman. (1997) International Hemoglobin Information Center Variant List. Hemoglobin 21:6, pages 505-506.
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. (1996) Variants of the Alpha Chain. Hemoglobin 20:3, pages 215-312.
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M. A.F. El-Hazmi. (1994) Genetic red cell disorders in saudi arabia: A multifaceted problem. Hemoglobin 18:3, pages 257-268.
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. (1994) International Hemoglobin Information Center. Hemoglobin 18:2, pages 77-161.
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. (1993) Variants of the Alpea Chain. Hemoglobin 17:2, pages 89-177.
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. (1992) Variants of the Alpha Chain. Hemoglobin 16:3, pages 127-213.
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. (1991) International hemoglobin information center: Variants of the alpha chain. Hemoglobin 15:3, pages 139-217.
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. (1990) International Hemoglobin Information Center. Hemoglobin 14:3, pages 249-325.
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. (1989) Variants of the Alpha Chain. Hemoglobin 13:3, pages 223-297.
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. (1988) IHIC Variants List. Hemoglobin 12:3, pages 209-282.
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. (1987) IHIC Variants List. Hemoglobin 11:3, pages 243-308.
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. (1986) International Hemoglobin Information Center IHIC Variants List. Hemoglobin 10:3, pages 261-327.
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. (1985) International Hemoglobin Information Center. Hemoglobin 9:3, pages 229-298.
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B. Al-Awamy, G. A. Niazi, J. B. Wilson & T. H. H. Huisman. (1985) Hb Setif or α294(G1)Asp→Tyrβ2 Observed in a Saudi Arabian Family. Hemoglobin 9:1, pages 87-90.
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. (1983) International Hemoglobin Information Center: Policies—Ihic. Hemoglobin 7:4, pages 331-406.
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. (1982) International Hemoglobin Information Center Policies - IHIC. Hemoglobin 6:3, pages 257-346.
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. (1981) International Hemoglobin Information Center Policies - Ihic. Hemoglobin 5:3, pages 259-323.
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I. Iuchi, K. Hidaka, T. Harano, S. Ueda, S. Shibata, S. Shimasaki, J. Mizushima, N. Kubo, T. Miyake & T. Uchida. (1980) Hemoglobin Takamatsu (β120 (GH 3) Lys → Gln): A New Abnormal Hemoglobin Detected in Three Unrelated Families in the Takamatsu Area of Shikoku. Hemoglobin 4:2, pages 165-176.
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. (1979) International Hemoglobin Information Center: Policies -Ihic. Hemoglobin 3:6, pages 481-513.
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P. H. Pinkerton, J. B. Wilson, H. Lam, D. Williams & T. H. J. Huisman. (1979) Hemoglobin Riyadh-β°-Thalassemia in an Indian Family. Hemoglobin 3:6, pages 451-458.
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. (1978) Variant Lists. Hemoglobin 2:6, pages 567-598.
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T. Miyaji, Y. Ohba, M. Matsunka, H. Kudoh, M. Asano, K. Yamaoto & T. Satoh. (1977) Hemoglobin Karatsu: Beta 120 (GH 3) Lysinc → Asparaine, an Example of Hb Riyadh in Japan. Hemoglobin 1:5, pages 461-466.
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Leslee J. Budge, Thomas B. Bradley & John L. Graham. (1977) Hemoglobin Riyadh in a Mexican American Famtly of Spanish Ancestry. Hemoglobin 1:3, pages 283-287.
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. (1977) International Hemoglobin Information Center. Hemoglobin 1:7, pages 707-733.
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Articles from other publishers (7)

Osama Alsmadi, Sumi E. John, Gaurav Thareja, Prashantha Hebbar, Dinu Antony, Kazem Behbehani & Thangavel Alphonse Thanaraj. (2014) Genome at Juncture of Early Human Migration: A Systematic Analysis of Two Whole Genomes and Thirteen Exomes from Kuwaiti Population Subgroup of Inferred Saudi Arabian Tribe Ancestry. PLoS ONE 9:6, pages e99069.
Crossref
L. Rigoli, A. Meo, M.R. Miceli, K. Alessio, R.A. Caruso, M.A. La Rosa, D.C. Salpietro, M. Ricca & I. Barberi. (2001) Molecular analysis of β-thalassaemia patients in a high incidence area of southern Italy. Clinical & Laboratory Haematology 23:6, pages 373-378.
Crossref
Mohsen A. F. El-Hazmi, Arjumand S. Warsy, Mohamed H. N. Addar & Zeinab Babae. (1994) Fetal haemoglobin level?effect of gender, age and haemoglobin disorders. Molecular and Cellular Biochemistry 135:2, pages 181-186.
Crossref
Y. Wada, A. Hayashi, Y. Oka, T. Matsuo, T. Sakurai, H. Matsuda & I. Katakuse. (1989) Mass spectrometric characterization of a haemoglobin variant, haemoglobin Riyadh. International Journal of Mass Spectrometry and Ion Processes 91:1, pages 79-84.
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J.B. Wilson, H. Lam, P. Pravatmuang & T.H.J. Huisman. (1979) Separation of tryptic peptides of normal and abnormal a, β, γ, and δ hemoglobin chains by high-performance liquid chromatography. Journal of Chromatography A 179:2, pages 271-290.
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M. A. F. El-Hazmi. (1979) On the nature of sickle-cell disease in the Arabian Peninsula. Human Genetics 52:3, pages 323-335.
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T. Arends, H. Lehmann, D. Plowman & R. Stathopoulou. (1977) Haemoglobin North Shore-Caracas β134 (H12) valine → glutamic acid. FEBS Letters 80:2, pages 261-265.
Crossref

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