Citations (61)
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Sona B. Nair, Arundhati S. Athalye, Madhavi Panphalia & Firuza R. Parikh. (2022) First Report of an α Chain Variant [Hb Coombe Park (HBA2: c.382A>G)] from India, Coinherited with a Novel SERPINC1 Gene Mutation: A Double Whammy?. Hemoglobin 46:5, pages 269-271.
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Lara Calcagno, Maria M. Ciriello, Monica Maccarini, Massimo Mogni, Massimo Maffei, Giuseppina Barberio, Sauro Maoggi, Domenico Coviello & Giovanni Ivaldi. (2022) Hb Alessandria [β37(C3)Trp→Leu; HBB: c.113G>T]: a Novel Variant on the β-Globin Chain with Slightly Increased Affinity for Oxygen Detected by Capillary Electrophoresis. Hemoglobin 46:4, pages 240-244.
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Ibrahim Al Nabhani, John C. Aneke, Madeleine Verhovsek, Barry Eng, Kevin H.M. Kuo, Leona C. Rudinskas & John S. Waye. (2020) Novel High Oxygen Affinity Hemoglobin Variant in a Patient with Polycythemia: Hb Kennisis [β85(F1)Phe→Leu (TTT>TTG); HBB: c.258T>G]. Hemoglobin 44:1, pages 10-12.
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Amudan J. Srinivasan, Clare Morkane, Daniel S. Martin & Ian J. Welsby. (2017) Should modulation of p50 be a therapeutic target in the critically ill?. Expert Review of Hematology 10:5, pages 449-458.
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Saskia Brunner-Agten, Thomas von Känel, Benno Röthlisberger, Charles Broquet & Andreas R. Huber. (2017) Hb Bakersfield (HBA1: c.151_152insGGAGCC): The Insertion of Arg-His Between Codons 49 and 50 of the α1-Globin Chain Leads to Increased Oxygen Affinity. Hemoglobin 41:1, pages 1-5.
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Margherita Vinciguerra, Cristina Passarello, Filippo Cassarà, Filippo Leto, Monica Cannata, Anna Crivello, Veronica Di Salvo, Aurelio Maggio & Antonino Giambona. (2016) Hb San Cataldo [β144(HC1)Lys→Thr; HBB: C.434A > C]: A New Hemoglobin Variant with Increased Affinity for Oxygen. Hemoglobin 40:4, pages 223-227.
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Ka Ling Rosalina Ip, Jason Chi-Chiu So, Man-Fai Law, Raymond S. M. Wong, Ho Chi Tam & Margaret H. L. Ng. (2016) Hb Tarrant [α126(H9)Asp→Asn; HBA2: c.379G > A (or HBA1)] in a Chinese Family as a Cause of Familial Erythrocytosis. Hemoglobin 40:4, pages 260-263.
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Anderson B. Collier$suffix/text()$suffix/text(), Lea M. Coon, Philip Monteleone, Samuel Umaru, Kenneth C. Swanson, James D. Hoyer & Jennifer L. Oliveira. (2016) A Novel β-Globin Chain Hemoglobin Variant, Hb Allentown [β137(H15)Val→Trp (GTG>TGG) HBB: c.412_413delinsTG, p.Val138Trp], Associated with Low Oxygen Saturation, Intermittent Aplastic Crises and Splenomegaly. Hemoglobin 40:2, pages 130-133.
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Guilaine Boursier, Sébastien Trouillier, Muriel Giansily Blaizot, Hélène Igual, Jean-François Schved & Patricia Aguilar Martinez. (2013) A New High Affinity Variant Hb Aurillac (β141Leu→Val). Hemoglobin 37:6, pages 584-588.
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Rachel M. Taliercio, Rendell W. Ashton, Leonard Horwitz, Kenneth C. Swanson, Patricia C. Wendt, James D. Hoyer & Jennifer L. Oliveira. (2013) Hb Grove City [β38(C4)Thr→Ser, ACC>AGC; HBB: c.116C>G]: A New Low Oxygen Affinity β Chain Variant. Hemoglobin 37:4, pages 396-403.
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Paloma Ropero, Fernando A. González, Elena Cela, Cristina Beléndez, Beatriz Pérez, Cristina Seri, Emilia Fontanes, Ana Villegas & Joaquin Díaz-Mediavilla. (2013) Erythrocytosis in a Child due to Hb Andrew-Minneapolis [β144(HC1)Lys→Asn (AAG>AAT or AAC)] Associated with a Spanish (δβ)0-Thalassemia. Hemoglobin 37:1, pages 48-55.
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Susumu Inoue, Jennifer L. Oliveira, James D. Hoyer & Mahesh Sharman. (2012) Symptomatic Erythrocytosis Associated with a Compound Heterozygosity for Hb Lepore-Boston-Washington (δ87-β116) and Hb Johnstown [β109(G11)Val→Leu, GTG>TTG]. Hemoglobin 36:4, pages 362-370.
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Yuko Cho, Susumu Iizuka, Yoshio Hatae, Kunihiko Kobayashi, Yukio Hattori, Yasuhiro Yamashiro & Tadashi Ariga. (2012) A 25-Year Observation of a Japanese Female Patient with Hb Nottingham who has Two Children with the Same Disorder. Hemoglobin 36:5, pages 446-455.
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Dima El-Sharkawi, Chris Fisher, Sachin Khambadkone, Adrian D. Stephens & John B. Porter. (2012) Secondary Erythrocytosis Due to Compound Homozygosity, but not Compound Heterozygosity, for Hb Luton and α-Thalassemia: A Family Study. Hemoglobin 36:1, pages 7-17.
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Jennifer L. Oliveira, Kenneth Swanson, Patricia Wendt, Thomas D. Caughey & James D. Hoyer. (2010) Hb Cambridge-MA [β144(HC1)-β146(HC3)Lys-Tyr-His→0 (HBB c.433 A>T)]: A New High Oxygen Affinity Variant. Hemoglobin 34:6, pages 565-571.
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Vassiliki Kalotychou, Revekka Tzanetea, Kostas Konstantopoulos, Ioannis Papassotiriou & Ioannis Rombos. (2010) Erythrocytosis Due to a Combination of the High Oxygen Affinity Hemoglobin Variant, Hb Olympia [β20(B2)Val→Met] with β- and α-Thalassemia Mutations: First Case in the Literature. Hemoglobin 34:4, pages 383-388.
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Nattiya Teawtrakul, Chittima Sirijirachai, Ganjana Chansung & Goonnapa Fucharoen. (2010) Compound Heterozygous Hb Tak/Hb E Causes Secondary Erythrocytosis in a Thai Family. Hemoglobin 34:2, pages 165-168.
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Philippe Joly, Philippe Lacan, Martine Bererd, Caroline Garcia, Isabelle Zanella-Cleon, Michel Becchi, Martine Aubry, Nicole Couprie & Alain Francina. (2009) Description of Two New α Variants: Hb Canuts [α85(F6)Asp→His (α1)] and Hb Ambroise Pare [α117(GH5)Phe→Ile (α2)]; Two New β Variants: Hb Beaujolais [β84(EF8)Thr→Asn] and Hb Monplaisir [β147 (Tyr-Lys-Leu-Ala-Phe-Phe-Leu-Leu-Ser-Asn-Phe-Tyr-158-COOH)] and One New δ Variant: Hb A2-North Africa [δ59(E3)Lys→Met]. Hemoglobin 33:3-4, pages 196-205.
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Liana Cuccia, Laura Saieva, Zelia Borsellino, Maria R. Marocco, Giovan B. Ruffo, Jean Riou & Marcello Capra. (2008) Hb Hinwil [β38(C4)Thr→Asn, ACC>AAC] Associated with β0-Thalassemia in a Sicilian Child. Hemoglobin 32:6, pages 582-587.
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Lynda Walker, Barry Eng, Andrew McFarlane & John S. Waye. (2007) High Oxygen Affinity Hemoglobin Variant in a Canadian Family: Hb Bunbury [β94(FG1)Asp→Asn, GAC→AAC]. Hemoglobin 31:1, pages 101-103.
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Claude Préhu, Jean Riou & Henri Wajcman. (2007) Hb Barika [α42(C7)Tyr→His (α2)] Leads to an α+-Thalassemia-like Syndrome. Hemoglobin 31:1, pages 17-22.
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Paloma Ropero, Carlos Fernández-Lago, Ana Villegas, Marta Polo, Marta Mateo, Asunción Mora & Fernando A. González. (2006) Hb LA Coruña [β38(C4)Thr→Ile]: A New Hemoglobin Variant Leading to Familial Polycythemia. Hemoglobin 30:3, pages 379-383.
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Zachary T. FitzHugh & Martin R. Schiller. (2023) Systematic Assessment of Protein C-Termini Mutated in Human Disorders. Biomolecules 13:2, pages 355.
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Epifania Rita Testa, Adriana Masotti, Patrizia Valeri, Luciana Geremia, Valeria Brunetta & Andrea Bontadini. (2022) Unusual finding of high oxygen affinity haemoglobinopathy treated with phlebotomy: A rare but predictable union. Transfusion and Apheresis Science 61:1, pages 103290.
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Mathilde Filser, Betty Gardie, Mathieu Wemeau, Patricia Aguilar-Martinez, Muriel Giansily-Blaizot & François Girodon. (2022) Importance of Sequencing HBA1, HBA2 and HBB Genes to Confirm the Diagnosis of High Oxygen Affinity Hemoglobin. Genes 13:1, pages 132.
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