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Hemoglobin|October 5, 2011
In vitro characterization of the α-thalassemia point mutation HBA2:c.95+1G>A [IVS-I-1(G>A) (α2)]Talal Qadah, Jill Finlayson, Reza GhassemifarHemoglobin|November 15, 2011
Sex steroid priming for induction of puberty in thalassemia patients with pulsatile reversible hypogonadotrophic hypogonadismRatna Chatterjee, Tarak Nath Mukhopadhyay, Sharmila Chandra, et al.Hemoglobin|November 1, 2011
Hypogonadotrophic hypogonadism and diminished gonadal reserve accounts for dysfunctional gametogenesis in thalassaemia patients with iron overload presenting with infertilityRekha Bajoria, Ratna ChatterjeeHemoglobin|November 1, 2011
Neurocognitive testing and functioning in adults sickle cell diseaseMiriam H Feliu, Regina D Crawford, Lekisha Edwards, et al.Hemoglobin|December 24, 2011
Analysis of the rs35959442 polymorphism in Hb E/β-thalassemia in Guangxi Province of the Republic of ChinaYunyan He, Ping Chen, Weixiong Lin, et al.Hemoglobin|January 6, 2012
Identification of a novel mutation in the β-globin gene 3' untranslated region [+1,506 (A>C)] in a Japanese male with a heterozygous β-thalassemia phenotypeMinako Hino, Yasuhiro Yamashiro, Yukio Hattori, et al.Hemoglobin|January 6, 2012
Secondary erythrocytosis due to compound homozygosity, but not compound heterozygosity, for Hb Luton and α-thalassemia: a family studyDima El-Sharkawi, Chris Fisher, Sachin Khambadkone, et al.Hemoglobin|February 24, 2012
Prevalence and molecular analysis of β-thalassemia in Adiyaman, TurkeyAhmet Genc, Deniz Tastemir Korkmaz, Mehmet Buyukleyla, et al.Hemoglobin|July 26, 2008
A rare thalassemic syndrome caused by interaction of Hb Adana [alpha59(E8)Gly-->Asp] with an alpha+-thalassemia deletion: clinical aspects in two casesVarvara Douna, Ioannis Papassotiriou, Anastasia Garoufi, et al.Hemoglobin|February 11, 2022
Hb Mizuho (HBB: c.206T>C): Pitfalls of Screening Tests in an Unstable Hemoglobin Variant Diagnosed after Targeted Next-Generation SequencingDiksha D Yadav, Manu Jamwal, Namrata Singh, et al.Pageof 240