Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Pain and HBG2[original query] |
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| DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease. Proceedings of the National Academy of Sciences of the United States of America 2008 Aug 105 (33): 11869-74. Lettre Guillaume, Sankaran Vijay G, Bezerra Marcos André C, Araújo Aderson S, Uda Manuela, Sanna Serena, Cao Antonio, Schlessinger David, Costa Fernando F, Hirschhorn Joel N, Orkin Stuart |
| Genetics of fetal hemoglobin in tribal Indian patients with sickle cell anemia. Translational research : the journal of laboratory and clinical medicine 2015 Jun 165 (6): 696-703. Bhanushali Aparna A, Patra Pradip K, Pradhan Smarnika, Khanka Suraj S, Singh Sujata, Das Bibhu |
| The Sickle ?-Thalassemia Phenotype. Journal of pediatric hematology/oncology 2017 Jan . Adekile Adekunle D, Akbulut Nagihan, Azab Asmaa F, Al-Sharida Sundus, Thomas Dia |
| The association of HBG2, BCL11A, and HMIP polymorphisms with fetal hemoglobin and clinical phenotype in Iraqi Kurds with sickle cell disease. International journal of laboratory hematology 2018 Sep . Al-Allawi Nasir, Qadir Shatha M A, Puehringer Helene, Chui David H K, Farrell John J, Oberkanins Christi |
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- Page last updated:Sep 18, 2023
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