References
- Kister J., Préhu C., Riou J., Godart C., Bardakdjian Promé D., Galactéros F., Wajcman H. Two hemoglobin variants with an alteration of the oxygen-linked chloride binding: Hb Antananarivo [α1(NA1)Val→Gly] and Hb Barbizon [β144(HCl)Lys→Met]. Hemoglobin 1999; 23: 21–32
- Hamaguchi K., Harano K., Harano T., Sakata T. HbOita [α45(CE3)His→Pro]: a new silent hemoglobin variant. Hemoglobin 1998; 22: 347–354
- Wajcman H., Promé D., Préhu C., Déon C., Riou J, Bouanga J. C., Papassotiriou I., Lahary A., Galactéros F. Hb Les Andelys [α83(F4)Leu→Pro]: a new moderately unstable variant. Hemoglobin 1998; 22: 129–140
- Agarwal S., Hattori Y., Gupta U. R., Agarwal S. S. A novel Indian β-thalassemia mutation: Hb Lucknow [β8(A5)Lys→Arg]. Hemoglobin. 1999, this issue
- Hojas-Bernal R., McNab-Martin P., Fairbanks V. F., Holmes M. W., Hoyer J. D., McCormick D. J., Kubik K. S. Hb Chile [β28(B10)Leu→Met]: an unstable hemoglobin associated with chronic methemoglobinemia and sulfonamide or methylene blue-induced hemolytic anemia. Hemoglobin 1999; 23: 125–134
- Grignoli C. R.E., Wenning M. R.S.C, Sonati M. F., Kimura E. M., Arruda V. R., Saad S. T.O., Costa F. F. Hb Rio Claro [β34(B16)Val→Met]: a novel electrophoretically silent variant found in association with Hb Hasharon [α47(CE5)Asp→His] and α-thalas-semia-2(-α37). Hemoglobin 1999; 23: 177–182
- Bento M. C., Ribeiro M. L., Cunha E., Rebelo U., Granjo E., Granado C., Tamagnini G. P. Hb Vila Real [β36(C2)Pro→His]: a newly discovered high oxygen affinity variant. Hemoglobin. 1999, in press
- Wajcman H., Riou J., Promé D., Kister J., Galactéros F. Hb Brie Comte Robert [β36(C2)Pro→Ala]: a new hemoglobin variant with high oxygen affinity and marked hydrophobic properties. Hemoglobin. 1999, this issue
- Nakanishi T., Miyazaki A., Kishikawa M, Shimizu A., Kishida O., Sumi S., Tsubakio T., Imai K. A new hemoglobin variant found during Hb A1c measurement: Hb Hokusetsu [β52(D3)Asp→Gly]. Hemoglobin 1998; 22: 355–371
- Hopmeier P., Plaseska-Karanfilska D., Efremov G. D. A new P chain variant, Hb Vienna or β77(EF1)His→-Gln. Hemoglobin 1998; 22: 391–395
- Frischknecht H., Speich R., Bloch K. E., Fehr J., Tuchschmid P., Jenni R. Hb Schlierbach or β108(G10)Asn→Ile: a new variant with low oxygen affinity detected in a Swiss family. Hemoglobin 1999; 23: 83–87
- Henthorn J. S., Mantio D., Davies S. C., Riou J., Wajcman Promé J., Galactéros F. Hb Brent [β117(G 19)His→-Asn]: a new hemoglobin variant found during routine antenatal screening. Hemoglobin 1999; 23: 89–93
- Henthorn J. S., Wajcman H., Promé D., Riou J., Kister J., Baudin-Creuza V., Davies S. C., Galactéros F. Hb Harrow [β118(GH1)Phe→Cys]: a new neutral hemoglobin variant. Hemoglobin. 1999, this issue
- Wajcman H., Kister J., Préhu C., Riou J., Godart C., Bardakdjian J., Soummer A. M., Promé D., Galactéros F. Hb Tende [β124(H2)Pro→Leu]: a new variant with a moderate increase in oxygen affinity. Hemoglobin 1998; 22: 517–523
- Miyazaki A., Nakanishi T., Kishikawa M., Nakagawa T., Shimizu A., Mohammed Mawjood A. H., Imai K., Aoki Y., Kikuchi M. Compound heterozygosity for β+-thalassemia [-31 (A→G)] and a new variant with low oxygen affinity. Hb Sagami [β139(H17) Asn→Thr] Hemoglobin. 1999, this issue
- van den Berg H. M., Bruin M. C.A., Batelaan D., van Delft P., van Zwieten R., Roos D., Harteveld C. L., Bernini L. F., Giordano P. C. Hb Nijkerk: a new mutation at codons 138/139 of the β-globin gene inducing severe hemolytic anemia in a Dutch girl. Hemoglobin 1999; 23: 135–144
- Li W., Hattori Y., Ohba Y., Okayama N., Lin W. S., Long G. F., Yamashiro Y., Yamamoto K U., Yamamoto K I. Another example of the β-thalassemia Mutation, IVS-I (-2) or codon 30 (A→G), found in a Chinese family. Hemoglobin 1998; 22: 377–381
- Pachcco P. 1999, Personal communication