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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Last data update: Jun 21, 2024
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Records 1 - 27 (of 27 Records)
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Performance of single-gene noninvasive prenatal testing for autosomal recessive conditions in a general population setting.
Julia Wynn et al. Prenat Diagn 2023
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α- and β-Globin Gene Mutations in Individuals with Hemoglobinopathies in the Chattogram and Sylhet Regions of Bangladesh.
Tamanna Kabir et al. Hemoglobin 2023 1-8
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[Diagnostics and treatment of alpha- and beta-thalassemias].
Cario Holger et al. Deutsche medizinische Wochenschrift (1946) 2022 147(19) 1250-1259
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Thalassemia in India.
Colah Roshan B et al. Hemoglobin 2022 46(1) 20-26
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Successful Implementation of Newborn Screening for Hemoglobin Disorders in the Philippines.
Padilla Carmencita D et al. International journal of neonatal screening 2021 7(2)
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Selecting β-thalassemia Patients for Gene Therapy: A Decision-making Algorithm.
Baronciani Donatella et al. HemaSphere 2021 5(5) e555
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Professionally responsible management of the ethical and social challenges of antenatal screening and diagnosis of β-thalassemia in a high-risk population.
Corda Valentina et al. Journal of perinatal medicine 2021
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β-Thalassemias.
Taher Ali T et al. The New England journal of medicine 2021 384(8) 727-743
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Thalassemias: An Overview.
Angastiniotis Michael et al. International journal of neonatal screening 2019 Mar 5(1) 16
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δ-Globin Chain Variants Associated with Decreased Hb A 2 Levels: A National Reference Laboratory Experience.
Rets Anton V et al. Hemoglobin 2020 Oct 1-4
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Gene Therapy of the Hemoglobinopathies.
Kunz Joachim B et al. HemaSphere 2020 Oct 4(5) e479
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Appropriate thresholds for accurate screening for β-thalassemias in the newborn period: results from a French center for newborn screening.
Allaf Bichr et al. Clinical chemistry and laboratory medicine 2020 Aug
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Investigating the suitability of high-resolution mass spectrometry for newborn screening: identification of hemoglobinopathies and β-thalassemias in dried blood spots.
Wiesinger Thomas et al. Clinical chemistry and laboratory medicine 2020 Feb
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Variations in prenatal screening in a US federal healthcare system: Same coverage, different options.
Thagard Andrew S et al. Journal of genetic counseling 2019 Sep
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Omics Studies in Hemoglobinopathies.
Katsantoni Eleni et al. Molecular diagnosis & therapy 2019 23(2) 223-234
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Molecular diagnostic update in hereditary hemolytic anemia and neonatal hyperbilirubinemia.
Rets Anton et al. International journal of laboratory hematology 2019 May 41 Suppl 195-101
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Beta Thalassemia: Monitoring and New Treatment Approaches.
Khandros Eugene et al. Hematology/oncology clinics of North America 2019 Jun 33(3) 339-353
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Recent progress in laboratory diagnosis of thalassemia and hemoglobinopathy: a study by the Korean Red Blood Cell Disorder Working Party of the Korean Society of Hematology.
Lee Young Kyung et al. Blood research 2019 Mar 54(1) 17-22
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Clinical Classification, Screening and Diagnosis for Thalassemia.
Viprakasit Vip et al. Hematology/oncology clinics of North America 2018 32(2) 193-211
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Incidence of hemoglobinopathies and thalassemias in Northern Alberta. Establishment of reference intervals for HbF and HbA2.
Rodriguez-Capote Karina et al. Clinical biochemistry 2015 Jul 48(10-11) 698-702
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Prevalence of Thalassemia among Newborns: A Re-visited after 20 Years of a Prevention and Control Program in Northeast Thailand.
Chaibunruang Attawut et al. Mediterranean journal of hematology and infectious diseases 2018 10(1) e2018054
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Hydroxyurea for hemoglobin E/β-thalassemia: a systematic review and meta-analysis.
Algiraigri Ali H et al. International journal of hematology 2017 Aug
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Hydroxyurea for nontransfusion-dependent β-thalassemia: A systematic review and meta-analysis.
Algiraigri Ali H et al. Hematology/oncology and stem cell therapy 2017 Apr
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The a-thalassemias.
Piel Frédéric B et al. N. Engl. J. Med. 2014 Nov 13. (20) 1908-16
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Progress Toward the Control and Management of the Thalassemias.
Fucharoen Suthat et al. Hematology/oncology clinics of North America 2016 Apr 30(2) 359-71
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Recent patents and technology transfer for molecular diagnosis of β-thalassemia and other hemoglobinopathies.
Breveglieri Giulia et al. Expert opinion on therapeutic patents 2015 Sep 1-24
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Effectiveness of Prenatal Screening for Hemoglobinopathies in a Developing Country.
Choudhuri Soumita et al. Hemoglobin 2015 May 13. 1-4
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Page last reviewed:
Feb 1, 2024
Page last updated:
Jun 21, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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