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Ekaterina Demidova, Valentina Salomashkina, Daria Selivanova, Evgeny Litvin, Natalia Karamyan, Svetlana Mann, Valentina Dvirnyk, Salia Maryina, Natal’ya Petrova, Lana Gorgidze, Anastasiya Peredel’skaya, Nina Tsvetaeva, Nataliya Smetanina & Vadim Surin. (2023) Hb Ryazan: An Elongated C‐Terminal β-Chain Due to a New Frameshift Mutation, HBB: c.396delG p.Val133Trpfs*25. Hemoglobin 47:2, pages 97-101.
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T. P. Molchanova, S. V. Kolledey, L. Ch. Pronina, O. A. Mirgorodskaya, A. Ch. Musolyamov, L. V. Abaturov & T. H. J. Huisman. (1999) Unstable Hb Newcastle [β92(F8)His→Pro], First Case Discovered in a Russian Patient. Hemoglobin 23:4, pages 373-378.
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W. C. Tsoi, C. K. Li, D. Plaseska-Karanfilska & G. D. Efremov. (1998) Hb Brockton [βl38(H16)Ala→Pro] Observed in a Chinese Boy. Hemoglobin 22:4, pages 397-400.
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T. P. Molchanova & T. H. J. Huisman. (1996) The Importance of the 3′ Untranslated Region for the Expression of the α-Globin Genes. Hemoglobin 20:1, pages 41-54.
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E. G. Kazanetz, J. Ye. Leonova, J. B. Wilson, S. K. McMillan, M. Walbrecht, J. Mi. de Pablos Gallego & T. H. J. Huisman. (1995) Hb ananosa or α2111(G18)Ala → Valβ (α2 Mutation) and Hb mulhacen or α2123(H6)Ala → Serβ2 (αl Mutation) are two silent stable variants detected by sequencing of amplified dna. Hemoglobin 19:1-2, pages 1-6.
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A. Gürgey, C. Altay, L.-H. Gu, J. Ye. Leonova, A. Delibalta, C. Öner & T. H. J. Huisman. (1995) HB Hakkari or α2β231(B13)LEU→ARG, A Severely Unstable Hemoglobin Variant Associated with Numerous Intra-Erythroblastic Inclusions and Erythroid Hyperplasia of the Bone Marrow. Hemoglobin 19:3-4, pages 165-172.
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J. T. Prchal, B. Adler, J. B. Wilson, E. Baysal, W.-B. Qin, T. P. Molchanova, D. D. Pobedimskaya, E. G. Kazanetz & T. H. J. Huisman. (1995) HB Bibba OR α2136(H19)LEU→PROβ2 in a Caucasian Family from Alabama. Hemoglobin 19:3-4, pages 151-164.
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P. L. Pande, S. Prakash, R. S. Tiwary, E. G. Kazanetz, J. Ye. Leonova & T. H.J. Huisman. (1995) β-Thalassemia Intermedia in An Indian Female h the Hb Hofu [β126(H4)Val→Glu]-(β°-Thalassemia [Codons 8/9 (+G)] Combination. Hemoglobin 19:5, pages 301-306.
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L-H. Gu, J. Ye. Leonova & T. H.J. Huisman. (1995) Hb S-Hb Lufkin Dise in A Black Male Infant. Hemoglobin 19:5, pages 291-294.
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W-B. Qin, D. D. Pobedimskaya, T. P. Molchanova, J. B. Wilson, L-H Gu, J.M de Pablos & T. H. J. Huisman. (1994) Hb Fannin-Lubbock in Five Spanish Families is Characterized by two Mutations: β111 GTC->CTC (VAL->LEU) AND β119 GGC->GAC (GLY->ASP). Hemoglobin 18:4-5, pages 297-306.
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T. P. Molchanova, Yu. V. Postnikov, D. D. Pobedimskaya, N. S. Smetanina, A. A. Moschan, E. G. Kazanetz, Yu. N. Tokarev & T. H. J. Huisman. (1993) HB Alesha or α2 β267(E11)VAL →MET: A New Unstable Hemoglobin Variant Identified Through Sequencing of, Amplified DNA. Hemoglobin 17:3, pages 217-225.
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V. Divoky, M. Svobodova, K. Indrak, L. Chrobak, T. P. Molchanova & T. H. J. Huisman. (1993) HB Hradec Kralove (HB HK) or α2 β2 115(617)ALA→ASP, A Severely Unstable Hewglobin Variant Resulting in a Dominant β-Thalassemia Trait in a Czech Family. Hemoglobin 17:4, pages 319-328.
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Articles from other publishers (7)
Titus H.J. Huisman. (1997) High performance liquid chromatographic analysis of human hemoglobins and their polypeptide chains: its use in the identification of variants. Analytica Chimica Acta 352:1-3, pages 187-200.
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W. E. Rodriguez Romero, M. Castillo, M. A. Chaves, G. F. Saenz, L. -H. Gu, J. B. Wilson, E. Baysal, N. S. Smetanina, J. Y. Leonova & T. H. J. Huisman. (1996) Hb Costa Rica or α2β277(EF1)His→Arg: The first example of a somatic cell mutation in a globin gene. Human Genetics 97:6, pages 829-833.
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G. R. Gray, H. E. Manson, L‐H. Gu, J. Ye. Leonova & T. H. J. Huisman. (2006)
Hb lulu island (α
2
β
2
107[G9]Gly→Asp)‐β°‐thalassemia (codon 15; TGG → TAG), a form of thalassemia intermedia
. American Journal of Hematology 50:1, pages 26-29.
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D. D. Pobedimskaya, T. P. Molchanova, S. Streichman & T. H. J. Huisman. (2006) Compound heterozygosity for two α‐globin gene defects, Hb taybe (α1; 38 or 39 minus thr) and a poly a mutation (α2; AATAAA → AATAAG), results in a severe hemolytic anemia. American Journal of Hematology 47:3, pages 198-202.
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T. P. Molchanova, D. D. Pobedimskaya & T. H. J. Huisman. (1994) The differences in quantities of α2-and α1-globin gene variants in heterozygotes. British Journal of Haematology 88:2, pages 300-306.
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M. A.çürük, T. P. Molchanova, Yu. V. Postnikov, D. D. Pobedimskaya, R. Liang, E. Baysal, S. Kolodey, N. S. Smetanina, Yu. N. Tokarev, A. G. Rumyantsev & T. H. J. Huisman. (1994) β-thalassemia alleles and unstable hemoglobin types among russian pediatric patients. American Journal of Hematology 46:4, pages 329-332.
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M. A. Çürük, A. J. Dimovski, E. Baysal, L‐H. Gu, F. Kutlar, T. P. Molchanova, B. B. Webber, Ç. Altay, A. Gürgey & T. H. J. Huisman. (2006)
Hb adana or α
2
59(E8)Gly→Aspβ
2
, A severely unstable α
1
‐globin variant, observed in combination with the ‐(α)20.5 KB α‐thal‐1 deletion in two Turkish patients
. American Journal of Hematology 44:4, pages 270-275.
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