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Hemoglobin|January 1, 1989
Hb Luxembourg [alpha 24(B5) Tyr----His]: a new unstable variantP Groff, F Galacteros, G Kalmes, et al.
Hemoglobin|January 1, 1989
Hemoglobin Windsor or beta 11 (A8)Val----Asp: a new unstable beta-chain hemoglobin variant producing a hemolytic anemiaA T Gilbert, P J Fleming, D R Sumner, et al.
Hemoglobin|January 1, 1989
Hb Bruxelles: alpha 2A beta (2)41 or 42(C7 or CD1)Phe deletedY Blouquit, J Bardakdjian, D Lena-Russo, et al.
Hemoglobin|June 30, 2015
The Prevalence of Hemoglobinopathies in Young Adolescents in the Province of Muğla in Turkey: Results of a Screening ProgramYaşar Topal, Hatice Topal, Mustafa Nuri Ceyhan, et al.
Hemoglobin|June 16, 2015
Molecular Basis of β-Thalassemia in the Population of the Aegean Region of Turkey: Identification of A Novel Deletion MutationFerda Ozkinay, Huseyin Onay, Emin Karaca, et al.
Hemoglobin|April 23, 2020
Multi-Locus Models to Address Hb F Variability in Portuguese β-Thalassemia CarriersLicínio Manco, Celeste Bento, Luís Relvas, et al.
Hemoglobin|June 9, 2020
XmnI Polymorphism in Sickle Cell Disease in North MoroccoFatima-Zahra Alaoui-Ismaili, Achraf Laghmich, Naima Ghailani-Nourouti, et al.
Hemoglobin|April 28, 2020
Hematological Characteristics of Hb Constant Spring (HBA2: c.427T>C) Carriers in Mainland ChinaFan Jiang, Li-Li Xu, Gui-Lan Chen, et al.
Hemoglobin|November 12, 2022
Knowledge and Attitude toward Hemoglobinopathies in Premarital Screening Program among the General Population in the Western Region of Saudi ArabiaHibah A Almasmoum, Aisha Tabassum, Mohammad Shahid Iqbal, et al.
Hemoglobin|January 1, 1991
Hb Westmead: an alpha 2-globin gene mutation detected by polymerase chain reaction and Stu I cleavageN H Jiang, S Liang, X J Wen, et al.
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