Hemoglobin

Hb Boskoop [HBA2c.112C>T p.Pro38Ser]: A New αα2 Chain Variant Observed in a Morrocan Family
pp. 97-102(6)
Authors: Versteegh, Florens G.A.; Arkesteijn, Sandra G.J.; Bakker-Verweij, Margreet; Haanappel, Karola; Delft, Peter van; Phylipsen, Marion; Kaufmann, Judith O.; Kok, Peter J.M.J.; Lansbergen, Gideon W.A.; Giordano, Piero C.; Harteveld, Cornelis L.

Hb Phimai [ββ72(E16)Ser→→Thr]: A Novel ββ-Globin Structural Variant Found in Association with Hb Constant Spring in Pregnancy
pp. 103-110(8)
Authors: Singsanan, Sanita; Srivorakun, Hataichanok; Fucharoen, Goonnapa; Puangplruk, Rawiwan; Fucharoen, Supan

Hb Sheffield [ββ58(E2)Pro→→His] in Oman: Potential Pitfall in Genetic Counseling
pp. 111-116(6)
Authors: Al Zadjali, Shoaib; Daar, Shahina; AlKindi, Salam; Gravell, David; Al Haddabi, Hamood; Berbar, Tsouria; Krishnamoorthy, Rajagopal

Hb A₂′′ (Hb B2) in the Omani Population and Diagnostic Significance
pp. 117-124(8)
Authors: Daar, Shahina; Al Zadjali, Shoaib; Gravell, David; Al Haddabi, Hamood; Al Riyami, Muna; Al Belushi, Abeer; Berbar, Tsouria; Krishnamoorthy, Rajagopal

Spectrum of ββ-Thalassemia Mutations in the Eastern Province of Saudi Arabia
pp. 125-134(10)
Authors: Al-Sultan, Ali; Phanasgaonkar, Supriya; Suliman, Ahmed; Al-Baqushi, Muneer; Nasrullah, Zaki; Al-Ali, Amein

Identical Mutations in the Paralogous Human γγ-Globin Genes Leading to Hemoglobin Variants and Nondeletional Hereditary Persistence of Fetal Hemoglobin
pp. 135-141(7)
Authors: Papachatzopoulou, Adamantia; Patrinos, George P.

Hb Lynwood [αα107(G14) (--T) (αα2) HBA2:c.323delT)] in Conjunction with the αα^3.7 Deletion Produces a Moderately Severe αα-Thalassemia Phenotype
pp. 142-146(5)
Authors: Finlayson, Jill; Ghassemifar, Reza; Holmes, Paula; Grey, Dianne; Newbound, Christopher; Pell, Nicole; Jennens, Michelle; Macaulay, Claire; Greenwood, Laura; Beilby, John

Two New Hemoglobin Variants: Hb Aix-Les-Bains [ββ5(A2)Pro→→Leu; HBB:c.17 C>T] and Hb Dubai [αα122(H5)His→→Leu (αα2); HBA2:c.368 A>T]
pp. 147-151(5)
Authors: Joly, Philippe; Garcia, Caroline; Lacan, Philippe; Couprie, Nicole; Francina, Alain

Detection of Hb Setif in North Iran and the Question of Its Origin: Iranian or Multiethnic??
pp. 152-156(5)
Authors: Mahdavi, Mohammad Reza; Karimi, Mehran; Yavarian, Majid; Roshan, Payam; Kosaryan, Mehrnoush; Siami, Rita

A Second Observation of the Rare Frameshift Mutation in the ββ-Globin Gene: Codon 46 (++A) (Hbb:c.138__139insA)
pp. 157-161(5)
Authors: Ghedira, Elyes Slim; Dupin-Deguine, Delphine; Duffilot, Denis; Lemetayer, Nathalie; Faubert, Emmanuelle; Pissard, Serge

Hb A₂ Hong Kong -- A Novel δδ-Globin Variant in a Chinese Family Masks the Diagnosis of ββ-Thalassemia Trait
pp. 162-165(4)
Authors: So, Chi-Chiu; Chan, Amy Y.Y.; Luo, Hong-Yuan; Verhovsek, Madeleine; Chui, David H.K.; Ling, Siu-Cheung; Chan, Li-Chong

Identification of a New αα Chain Variant at Codons 22--25 (--9 nts) Using the Sebia Capillarys 2 Electrophoresis System
pp. 166-170(5)
Authors: Liao, Can; Zhou, Jian-Ying; Xie, Xing-Mei; Liu, Ying-Na; Chen, Li-He; Li, Dong-Zhi

Bilirubin Peak can be Mistaken as Hb Bart's or Hb H on High-Performance Liquid Chromatography
pp. 171-174(4)
Authors: Kar, Rakhee; Sharma, Chaggan Bihari

Iron Chelation Therapy in Hereditary Hemochromatosis and Thalassemia Intermedia: Regulatory and Non Regulatory Mechanisms of Increased Iron Absorption [Kontoghiorghes GJ, Spyrou A, Kolganou A. Hemoglobin. 2010;34(3); 251--264]
pp. 175-179(5)
Author: Nick, H.P.