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Hemoglobin|August 20, 2015
The Spectrum of α-Thalassemia Mutations in Kermanshah Province, West IranReza Alibakhshi, Masomeh Mehrabi, Leila Omidniakan, et al.Hemoglobin|August 20, 2015
Frequencies of HKαα and anti-HKαα Alleles in Chinese Carriers of Silent Deletional α-ThalassemiaMan-Yu Wu, Jian Li, Shu-Chen Li, et al.Hemoglobin|August 21, 2015
Hb G-Waimanalo [A1] [α64(E13)Asp→Asn; HBA1: c.193 G > A] with Decreased Oxygen AffinityAxel Karow, Julia J M Eekels, Karin Zurbriggen, et al.Hemoglobin|August 21, 2015
A Novel Heme Pocket Hemoglobin Variant Associated with Normal Hematology: Hb Zara or α91(FG3)Leu→Ile (α2) (HBA2: c.274C > A)Sandro Trova, Paolo Mereu, Luca Decandia, et al.Hemoglobin|August 21, 2015
Identification of a Rare β(0)-Thalassemia Mutation, Codon 54 (-T) (HBB: c.165delT) in an Iranian FamilyNadia Ghasemian Dastjerdy, Ali Banihashemi, Mandana Azizi, et al.Hemoglobin|April 28, 2016
Spectrum of Common α-Globin Deletion Mutations in the Southern Region of VietnamLy Bui Thi Kim, Dung Phu Chi, Chi Hoang ThanhHemoglobin|April 28, 2016
Mild Microcytic Anemia in an Infant with a Compound Heterozygosity for Hb C (HBB: c.19G > A) and Hb Osu Christiansborg (HBB: c.157G > A)Maria O Boucher, David H K Chui, Bruce A Woda, et al.Hemoglobin|April 28, 2016
The Natural History of Hb S/Hereditary Persistence of Fetal Hemoglobin in 13 Children from the State of Minas Gerais, BrazilAndré R Belisário, Rahyssa R Sales, Célia M Silva, et al.Hemoglobin|December 31, 2014
Primer-introduced restriction analysis polymerase chain reaction method for non-invasive prenatal testing of β-thalassemiaSaijun Liu, Liyuan Chen, Xiandong Zhang, et al.Hemoglobin|March 23, 2013
Variable presentation of HB H disease due to homozygosity for the rare polyadenylation signal A T(Indian) (AATAAA>AATA- -) mutation in four Indian familiesSona B Nair, Anita H Nadkarni, Kanjaksha Ghosh, et al.Pageof 238