Human Genome Epidemiology Literature Finder
Records 1 - 17 (of 17 Records) |
Query Trace: Thalassemia and HBD[original query] |
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Is high pressure liquid chromatography an effective screening tool for characterization of molecular defects in hemoglobinopathies? Indian journal of pathology & microbiology 0 56 (1): 36-9. Moorchung Nikhil, Phillip Joseph, Sarkar Ravi Shankar, Prasad Rupesh, Dutta Vib |
First report of the spectrum of d-globin gene mutations in Omani subjects - identification of novel mutations. International journal of laboratory hematology 2015 Apr 37 (2): 238-43. Alkindi S, AlZadjali S, Daar S, Ambusaidi R, Gravell D, Al Haddabi H, Krishnamoorthy R, Pathare |
Characterization of Hb Lepore variants in the UK population. Hemoglobin 2015 39 (1): 58-61. Guo Lina, Kausar Anika, Old John M, Henderson Shirley J, Gallienne Alice |
Coinheritance of a Rare Nucleotide Substitution on the ß-Globin Gene and Other Known Mutations in the Globin Clusters: Management in Genetic Counseling. Hemoglobin 2016 Jun 1-5. Vinciguerra Margherita, Passarello Cristina, Leto Filippo, Crivello Anna, Fustaneo Maria, Cassarà Filippo, Cannata Monica, Maggio Aurelio, Giambona Antoni |
Sickle Cell Disease in Central India: A Potentially Severe Syndrome. Indian journal of pediatrics 2016 Apr . Jain Dipty, Warthe Vinit, Dayama Paridhi, Sarate Dilip, Colah Roshan, Mehta Pallavi, Serjeant Grah |
Diagnosis of Compound Heterozygous Hb Tak/?-Thalassemia and HbD-Punjab/?-Thalassemia by HbA Levels on Capillary Electrophoresis. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2018 2 34 (1): 110-114. Panyasai Sitthichai, Sakkhachornphop Supachai, Pornprasert Sako |
Hemoglobin A (HbA) has a measure of unreliability in diagnosing ?-thalassemia trait (?-TT). Current medical research and opinion 2018 2 34 (5): 945-951. Al-Amodi Amani M, Ghanem Neda Z, Aldakeel Sumayh A, Ibrahim Al Asoom Lubna, Rafique Ahmed Nazish, Almandil Noor B, Naserullah Zaki A, Al-Jarrash Sana, Shakil Akhtar Mohammed, AbdulAzeez Sayed, Al-Ali Amein K, Borgio J Franc |
Borderline hemoglobin A levels in northern Thai population: HBB genotypes and effects of coinherited alpha-thalassemia. Blood cells, molecules & diseases 2018 10 74 13-17. Chaweephisal Phumin, Phusua Arunee, Fanhchaksai Kanda, Sirichotiyakul Supatra, Charoenkwan Piml |
Molecular and geographical heterogeneity of hemoglobinopathy mutations in Azerbaijanian populations. Annals of human genetics 2019 Nov . Aliyeva Gunay, Asadov Chingiz, Mammadova Tahira, Gafarova Surmaya, Guliyeva Yegana, Abdulalimov Eld |
Hemoglobin variants in southern China: results obtained during the measurement of glycated hemoglobin in a large population. Clinical chemistry and laboratory medicine 2020 Jul . Xu Anping, Chen Weidong, Xie Weijie, Wang Yajun, Ji Li |
Association of Hb A Variants with Several Forms of ?- and ?-Thalassemia in Thailand. Hemoglobin 2020 6 44 (3): 179-183. Panyasai Sitthichai, Pornprasert Sako |
Association of polymorphisms in the HBG1-HBD intergenic region with HbF levels. Journal of clinical laboratory analysis 2020 Feb e23243. Hu Li, Huang Ling, Han Yuanyuan, Jin Tingting, Liu Juan, Jiang Minmin, Liu Xingmei, Li Yuanyuan, Han Wenping, An Bangquan, Huang Shengw |
Nationwide carrier detection and molecular characterization of ?-thalassemia and hemoglobin E variants in Bangladeshi population. Orphanet journal of rare diseases 2020 1 15 (1): 15. Noor Farjana Akther, Sultana Nusrat, Bhuyan Golam Sarower, Islam Md Tarikul, Hossain Mohabbat, Sarker Suprovath Kumar, Islam Khaleda, Khan Waqar Ahmed, Rahman Mujahida, Qadri Syeda Kashfi, Shekhar Hossain Uddin, Qadri Firdausi, Qadri Syed Saleheen, Mannoor Kaiiss |
Vitamin D level, lipid profile, and vitamin D receptor and transporter gene variants in sickle cell disease patients from Kurdistan of Iraq. Journal of clinical laboratory analysis 2021 7 35 (9): e23908. Hama Abdalla Hussein, Shakiba Ebrahim, Rahimi Zohreh, Karimi Mehran, Mozafari Hadi, Abdulkarim Omed Adn |
A New Mutation, Hb A-Canakkale [?10(A7)Ala?Val; HBD: c.32C>T], and Other Well-Known ? Variants Identified in a Selected Cohort with Low Hb A Levels. Hemoglobin 2022 8 46 (2): 87-90. Karakaya Taner, Silan Fatma, Ozdemir Oztu |
Detecting rare thalassemia in children with anemia using third-generation sequencing. Hematology (Amsterdam, Netherlands) 2023 8 28 (1): 2241226. Zhen-Min Ren, Wu-Jiao Li, Zhi-Hao Xing, Xiao-Ying Fu, Ju-Yan Zhang, Yun-Sheng Chen, De-Fa |
Mutational analysis of hemoglobin genes and functional characterization of detected variants, through in-silico analysis, in Pakistani beta-thalassemia major patients. Scientific reports 2023 8 13 (1): 13236. Samina Ejaz, Iqra Abdullah, Muhammad Usman, Muhammad Arslan Iqbal, Sidra Munawar, Muhammad Irfan Khan, Nagina Imtiaz, Hanniah Tahir, Muhammad Ihsan Bari, Tayyaba Rasool, Aneeza Fatima, Ramsha Anwar, Ayman Durrani, Yasir Hame |
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- Page last updated:Apr 16, 2024
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