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Hemoglobin|October 26, 2012
Influence of BCL11A, HBS1L-MYB, HBBP1 single nucleotide polymorphisms and the HBG2 XmnI polymorphism On Hb F levelsPapai Roy, Gargi Bhattacharya, Amrita Mandal, et al.Hemoglobin|October 31, 2012
A novel β(0)-thalassemia frameshift mutation: [HBB:c.216delT]Christopher Konialis, Birgitta Hagnefelt, Sophia Sevastidou, et al.Hemoglobin|January 1, 1987
Elevated G gamma gene expression with specific beta S gene haplotype, normal gamma gene maps and presence of the Xmn I site -158 5' to the G gamma gene in Indian sickle cell anemiaL E Lie-Injo, M L Lim, Z Randhawa, et al.Hemoglobin|May 16, 2014
A case series of α-thalassemia intermedia due to compound heterozygosity for Hb Adana [HBA2: c179G>A (or HBA1); p.Gly60Asp] with other α-thalassemias in Malay familiesHafiza Alauddin, Noor-Adilah Jaapar, Raja Z Azma, et al.Hemoglobin|June 19, 2014
Comparison of patients from Nigeria and the USA highlights modifiable risk factors for sickle cell anemia complicationsTitilola S Akingbola, Bamidele O Tayo, Babatunde Salako, et al.Hemoglobin|August 14, 2012
Low dose hydroxyurea is effective in reducing the incidence of painful crisis and frequency of blood transfusion in sickle cell anemia patients from eastern IndiaDilip K Patel, Ranjeet S Mashon, Siris Patel, et al.Hemoglobin|September 5, 2012
The spectrum of α- and β-thalassemia mutations in Yunnan Province of Southwestern ChinaJie Zhang, Bao-Sheng Zhu, Jing He, et al.Hemoglobin|September 6, 2012
A new hemoglobin variant: Hb Izmir [β86(F2)Ala→Val, GCC>GTC; HBB:c.260C>T]Aydan Çelebiler, Derya Aksoy, Serkan Ocakcı, et al.Hemoglobin|September 8, 1998
A new hemoglobin variant found during Hb A1c measurement: Hb Hokusetsu [beta52(D3)Asp-->Gly]T Nakanishi, A Miyazaki, M Kishikawa, et al.Pageof 240