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Hemoglobin
international journal for hemoglobin research
Volume 19, 1995 - Issue 1-2
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BriefNote Article

Compound heterozygosity for two β chain variants Hb S [β6(A3)Glu → val] and the high affinity variant Hb san diego [β109(G11)Val → met]

D. Williamson Department of Haematology, University of Cambridge Medical Research Council Centre, Cambridge, CB2 2QH, England
,
D. J. Perry Department of Haematology, University of Cambridge Medical Research Council Centre, Cambridge, CB2 2QH, England
,
K. Brown Department of Haematology, Addenbrookes National Health Service Trust, Cambridge CB2 2QQ England
,
J. V. Langdown Department of Haematology, Addenbrookes National Health Service Trust, Cambridge CB2 2QQ England
&
C. de Silva Department of Haematology, Whipps Cross Hospital Leytonstone, London E11 1NT England
Pages 27-32 | Received 19 Aug 1994, Accepted 05 Jan 1995, Published online: 07 Jul 2009

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Read on this site (5)

Thein Hlaing Oo. (2021) Secondary erythrocytosis due to hemoglobin San Diego. Baylor University Medical Center Proceedings 34:1, pages 159-160.
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P. Lacan, J. Drai, M. Aubry, A. Francina & J. Orgiazzi. (2000) A New β-Globin Variant: Hb Sainte Eugénie [β104(G6)Arg→Trp] in a French Caucasian Female. Hemoglobin 24:3, pages 245-248.
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P. Lacan, M. Aubry, A. Francina, N. Couprie, L. Dementhon & M. Becchi. (1999) Characterization of Hb djeifa [β98(FG5)Val→Ala] by DNA sequencing in a French caucasian family. Hemoglobin 23:1, pages 73-77.
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P. Lacan, M. Aubry, A. Francian & A. Lachaux. (1997) HB Zengcheng [β114(G16)LEU→MET] in a Cambodian Family. Hemoglobin 21:4, pages 363-367.
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D. Williamson, K. P. Brown, J. V. Langdown & T. P. Baglin. (1997) Mild Thalassemia Intermedia Resulting from a New Insertion/Frameshift Mutation in the β-Globin Gene. Hemoglobin 21:6, pages 485-493.
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Articles from other publishers (4)

Barbara Manconi, Maria Cristina De Rosa, Maria Pia Cappabianca, Alessandra Olianas, Cristiana Carelli Alinovi, Fabrizio Mastropietro, Donatella Ponzini, Antonio Amato & Mariagiuseppina Pellegrini. (2010) A new β-chain haemoglobin variant with increased oxygen affinity: Hb Roma [β115(g17)Ala→Val]. Biochimica et Biophysica Acta (BBA) - General Subjects 1800:3, pages 327-335.
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Paloma Ropero, Ana Villegas & Fernando A. González. (2004) Hemoglobinopatia Korle-Bu [β73(E17)Asp→Asn]. Primeros casos descritos en España. Medicina Clínica 123:7, pages 260-261.
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P. Ropero, A. Villegas, A.F. Gonz�lez, E. Anguita, J. S�nchez, D.L. Carre�o, B. Arrizabalaga & L. Atuxta. (2000) Hb Johnstown [?109 (G11) Val?Leu]: Second case described and associated for the first time with ?0-thalassemia in two Spanish families. American Journal of Hematology 65:4, pages 298-301.
Crossref
Titus Hendrik Jan Huisman. (1997) Combinations of β chain abnormal hemoglobins with each other or with β-thalassemia determinants with known mutations: influence on phenotype. Clinical Chemistry 43:10, pages 1850-1856.
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