Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jun 6, 2023. (Total: 217697Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 11 (of 11 Records)

Query Trace: Hemoglobinopathies and Hbb[original query]
Distinctive mutation spectrum of the HBB gene in an urban eastern Indian population.
Hemoglobin 2014 38 (1): 33-8.
Sahoo Subhransu Sekhar, Biswal Sebaranjan, Dixit Manjus
Frequency and spectrum of hemoglobinopathy mutations in a Uruguayan pediatric population.
Genetics and molecular biology 2013 Sep 36 (3): 316-22.
Luz Julio Da, Avila Amalia, Icasuriaga Sandra, Gongóra María, Castillo Luis, Serrón Alejandra, Kimura Elza Miyuki, Costa Fernando Ferreira, Sans Mónica, Sonati Maria de Fáti
Molecular diagnostics of the HBB gene in an Omani cohort using bench-top DNA Ion Torrent PGM technology.
Blood cells, molecules & diseases 2014 Sep 53 (3): 133-7.
Hassan S M, Vossen R H A M, Chessa R, den Dunnen J T, Bakker E, Giordano P C, Harteveld C
Newborn Screening for Hemoglobinopathies and Red Cell Enzymopathies in Tripura State: A Malaria-Endemic State in Northeast India.
Hemoglobin 2018 2 42 (1): 43-46.
Upadhye Dipti, Das Rajat S, Ray Jayanta, Acharjee Shukdeb, Ghosh Kanjaksha, Colah Roshan B, Mukherjee Malay
Role of Genomic Biomarkers in Increasing Fetal Hemoglobin Levels Upon Hydroxyurea Therapy and in ?-Thalassemia Intermedia: A Validation Cohort Study.
Hemoglobin 2019 5 43 (1): 27-33.
Kolliopoulou Alexandra, Siamoglou Stavroula, John Anne, Sgourou Argyro, Kourakli Alexandra, Symeonidis Argiris, Vlachaki Efthymia, Chalkia Panagiota, Theodoridou Stamatia, Ali Bassam R, Katsila Theodora, Patrinos George P, Papachatzopoulou Adamant
The Spectrum of ß-Thalassemia Mutations in Hamadan Province, West Iran.
Hemoglobin 2019 May 1-5.
Alibakhshi Reza, Moradi Keivan, Aznab Mozaffar, Azimi Azam, Shafieenia Samaneh, Biglari Mosta
?-Globin Gene Mutations in Pediatric Patients with ?-Thalassemia in the Region of Çukurova, Turkey.
Hemoglobin 2020 Jul 1-5.
Guzelgul Figen, Seydel G Seyda, Aksoy Kiym
Fetal hemoglobin regulating genetic variants identified in homozygous (HbSS) and heterozygous (HbSA) subjects from South Mexico.
Journal of tropical pediatrics 2022 9 68 (5): .
Rizo-de la Torre L C, Borrayo-López F J, Perea-Díaz F J, Aquino E, Venegas M, Hernández-Carbajal C, Espinoza-Mata L L, Ibarra-Cortés
Epidemiological and molecular study of hemoglobinopathies in Mauritanian patients.
Molecular genetics & genomic medicine 2022 9 10 (10): e2048.
Mahmoud Taher, Sahli Chaima, Hadj Fredj Sondess, Amri Yessine, Othmani Rim, Mohamed Ghaber S, Zein Ekhtelbenina, Messaoud Tai
Molecular prevalence of HBB-associated hemoglobinopathy among reproductive-age adults and the prenatal diagnosis in Jiangxi Province, southern central China.
Frontiers in genetics 2022 10 13 992073.
Luo Haiyan, Huang Ting, Lu Qing, Zhang Liuyang, Xu Yonghua, Yang Yan, Guo Zhen, Yuan Huizhen, Shen Yinqin, Huang Shuhui, Yang Bicheng, Zou Yongyi, Liu Yanq
?- and ?-Globin Gene Mutations in Individuals with Hemoglobinopathies in the Chattogram and Sylhet Regions of Bangladesh.
Hemoglobin 2023 3 1-8.
Kabir Tamanna, Anwar Saeed, Mourosi Jarin Taslem, Akter Shanjida, Hosen Mohammad Jak
TOP