HuGE Literature Finder
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Records 1-4
A single nucleotide polymorphism in the HBBP1 gene in the human ?-globin locus is associated with a mild ?-thalassemia disease phenotype.
Hemoglobin 2012 36 (5): 433-45. Giannopoulou Emily, Bartsakoulia Marina, Tafrali Christina, Kourakli Alexandra, Poulas Konstantinos, Stavrou Eleana F, Papachatzopoulou Adamantia, Georgitsi Marianthi, Patrinos George |
Influence of BCL11A, HBS1L-MYB, HBBP1 single nucleotide polymorphisms and the HBG2 XmnI polymorphism On Hb F levels.
Hemoglobin 2012 36 (6): 592-9. Roy Papai, Bhattacharya Gargi, Mandal Amrita, Dasgupta Uma B, Banerjee Debasis, Chandra Sarmila, Das Manikanch |
A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E.
![]() Human genetics 2010 Mar 127 (3): 303-14. Nuinoon Manit, Makarasara Wattanan, Mushiroda Taisei, Setianingsih Iswari, Wahidiyat Pustika Amalia, Sripichai Orapan, Kumasaka Natsuhiko, Takahashi Atsushi, Svasti Saovaros, Munkongdee Thongperm, Mahasirimongkol Surakameth, Peerapittayamongkol Chayanon, Viprakasit Vip, Kamatani Naoyuki, Winichagoon Pranee, Kubo Michiaki, Nakamura Yusuke, Fucharoen Suth |
A genome-wide association identified the common genetic variants influence disease severity in beta(0)-thalassemia/hemoglobin E.
Human genetics 2009 Nov . Nuinoon M, Makarasara W, Mushiroda T, Setianingsih I, Wahidiyat PA, Sripichai O, Kumasaka N, Takahashi A, Svasti S, Munkongdee T, Mahasirimongkol S, Peerapittayamongkol C, Viprakasit V, Kamatani N, Winichagoon P, Kubo M, Nakamura Y, Fucharoen S |
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