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Hemoglobin|September 13, 2018
Preventable Severe Thalassemia among ChildrenChaiwat Rerkswattavorn, Nongnuch Sirachainan, Duantida Songdej, et al.Hemoglobin|September 13, 2018
Compound Heterozygosity for Silent Cap +1570 (T>C) (HBB: c*96T>C), Codon 39 (C>T) (HBB: c.118C>T) and the Presence of αααStamatia Theodoridou, Timoleon-Achilleas Vyzantiadis, Efthymia VlachakiHemoglobin|May 31, 2019
The Sub-Phenotypes of Sickle Cell Disease in KuwaitAdekunle D Adekile, Sondus Al-Sherida, Rajaa Marouf, et al.Hemoglobin|May 18, 2019
The Spectrum of β-Thalassemia Mutations in Hamadan Province, West IranReza Alibakhshi, Keivan Moradi, Mozaffar Aznab, et al.Hemoglobin|May 1, 2019
A Case Report of Compound Heterozygosity for β0/β+-Thalassemia Resulting from under Diagnosed β-Thalassemia Found in a Hb A'2 SampleNutjeera Intasai, Ampai Phasit, Sitthichai Panyasai, et al.Hemoglobin|May 16, 2019
The Role of Exercise Stress Echocardiography for Determination of Subclinical Cardiac Involvement in β-Thalassemia MajorMozhgan Parsaee, Hamidreza Pouraliakbar, Azita Azarkeivan, et al.Hemoglobin|May 16, 2019
Severe Thalassemia Caused by Hb Zunyi [β147(HC3)Stop→Gln; HBB: c.442T>C)] on the β-Globin GeneQiong Su, Shiping Chen, Liusong Wu, et al.Hemoglobin|May 21, 2019
Compound Heterozygote for a Novel Elongated C-Terminal β-Globin Variant (HBB: c.364delG) and Hb E (HBB: c.79G>A) with Heterozygous α-Thalassemia-2Manit Nuinoon, Orapan Thipthara, Suthat FucharoenHemoglobin|January 1, 1976
Another form of the hereditary persistence of fetal hemoglobin (the Atlanta type)?C Altay, T H Huisman, W A SchroederHemoglobin|January 1, 1976
Homozygous cases for hemoglobin J Mexico (alpha54 (E3)Gln replaced by Glu) evidence for a duplicated alpha gene with unequal expressionG Trabuchet, J Pagnier, M Benabadji, et al.Pageof 239