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Hemoglobin|January 1, 1991
Hb Geelong [beta 139(H17)Asn----Asp]P F Como, D R Hocking, G W Swinton, et al.
Hemoglobin|December 10, 2008
alpha-thalassemia mutations in Khuzestan Province, Southwest IranKhodamorad Zandian, Jamal Nateghi, Bijan Keikhaie, et al.
Hemoglobin|December 10, 2008
Neonatal cyanosis due to a novel fetal hemoglobin: Hb F-Circleville [Ggamma63(E7)His-->Leu, CAT>CTT]Erin Dainer, Richard Shell, Randy Miller, et al.
Hemoglobin|January 1, 1990
Sickle cell anemia and major organ failureD R Powars
Hemoglobin|January 1, 1990
Hb Davenport or alpha 2(78)(EF7)Asn----His beta 2J B Wilson, B B Webber, D Plaseska, et al.
Hemoglobin|February 13, 2013
Normal Hb A2 β-thalassemia trait: frameshift mutation (HBB: c.187_251dup) in cis with the Hb A2' δ-globin gene missense mutation (HBD: c.49G>C)John S Waye, Barry Eng, Laurie Hellens, et al.
Hemoglobin|April 17, 2013
Silent β-thalassemia mutations at -101 (C>T) and -71 (C>T) and their coinheritance with the sickle cell mutation in BahrainNabeel J Al Moamen, Fawzia Mahdi, Ebtihal Salman, et al.
Hemoglobin|April 18, 2013
Maternal complications and the association with baseline variables in pregnant women with sickle cell diseaseSharifa H Al-Farsi, Nihal M Al-Riyami, Murtadha K Al-Khabori, et al.
Hemoglobin|March 9, 2013
Codon 62 (GTG>GCG, Val→Ala) (α1) (HBA1: c.188T>C) causing nondeletional α-thalassemia in a Chinese familyCan Liao, Hai-Shen Tang, Ru Li, et al.
Hemoglobin|January 1, 1977
Hemoglobin Lufkin: beta 29 (B11) Gly replaced by Asp. An unstable hemoglobin variant involving an internal amino acid residueR M Schmidt, K C Bechtel, M H Johnson, et al.
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