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1. Hemoglobin
Hemoglobin, ISSN 1532-432X, 1976
Hemoglobin | Hemoglobinopathy | Periodicals
Journal
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2. Variant haemoglobins
: a guide to identification
by Bain, Barbara J
2010, ISBN 9781444329773, vi, 254
Hemoglobinopathy | Hemoglobinopathies | genetics | Hemoglobin polymorphisms | diagnosis | Identification | Hemoglobins | Hemoglobinopathy - Genetic aspects | Hemoglobinopathies - diagnosis | Hemoglobinopathy - Diagnosis | Hemoglobin | Hemoglobins - genetics | Diagnosis | Hemoglobin polymorphisms - Identification
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3. Full Text The inherited diseases of hemoglobin are an emerging global health burden
by Weatherall, David J
Blood, ISSN 0006-4971, 06/2010, Volume 115, Issue 22, pp. 4331 - 4336
Life Sciences & Biomedicine | Hematology | Science & Technology | Hematologic and hematopoietic diseases | Biological and medical sciences | Medical sciences | Hemoglobinopathies - therapy | Genetics, Population | Global Health | Hemoglobinopathies - diagnosis | Humans | Hemoglobinopathies - genetics | Developing Countries | Epidemiologic Factors | Infant, Newborn | Hemoglobinopathies - epidemiology | Index Medicus | Abridged Index Medicus | s
Journal Article
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4. Full Text Wide range of F cell levels in healthy Thai adults: Influence of Swiss-type hereditary persistence of foetal haemoglobin & β-haemoglobinopathy
by Tatu, Thanusak
Indian journal of medical research (New Delhi, India : 1994), ISSN 0971-5916, 2/2019, Volume 150, Issue 2, pp. 161 - 166
Immunology | Life Sciences & Biomedicine | Medicine, General & Internal | General & Internal Medicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Anemia, Sickle Cell - pathology | beta-Thalassemia - pathology | beta-Thalassemia - epidemiology | Erythrocyte Indices - genetics | Humans | beta-Thalassemia - genetics | Child, Preschool | Hemoglobinopathies - blood | Infant | Male | Thailand | Hemoglobin E - genetics | Blood Donors | Anemia, Sickle Cell - epidemiology | Hemoglobinopathies - genetics | Adult | Female | Infant, Newborn | beta-Thalassemia - blood | Hemoglobinopathies - epidemiology | Hemoglobinopathies - pathology | Phenotype | Fetal Hemoglobin - genetics | Heterozygote | Anemia, Sickle Cell - blood | Anemia, Sickle Cell - genetics | Studies | Automation | Blood & organ donations | Hemoglobin | Mutation | Gene expression | Males | Blood banks | Polymorphism | Index Medicus | F cell | ß-thalassaemia | haemoglobinopathies | ß-hemoglobinopathy | Original | Swiss-type HPFH | β-hemoglobinopathy - β-thalassaemia - f cell - haemoglobinopathies - swiss-type hpfh
Journal Article
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5. Full Text Challenges of alloimmunization in patients with haemoglobinopathies
by Chou, Stella T and Liem, Robert I and Thompson, Alexis A
British journal of haematology, ISSN 0007-1048, 11/2012, Volume 159, Issue 4, pp. 394 - 404
transfusion | haemoglobinopathies | thalassaemia | alloimmunization | sickle cell disease | Thalassaemia | Transfusion | Sickle cell disease | Haemoglobinopathies | Alloimmunization | Life Sciences & Biomedicine | Hematology | Science & Technology | Hematologic and hematopoietic diseases | Anemias. Hemoglobinopathies | Biological and medical sciences | Medical sciences | Diseases of red blood cells | Erythrocytes - immunology | Thalassemia - therapy | Thalassemia - blood | Erythrocyte Transfusion - adverse effects | Prevalence | Humans | Risk Factors | Hemoglobinopathies - blood | Thalassemia - immunology | Hemoglobinopathies - immunology | Hemoglobinopathies - therapy | Isoantibodies - blood | Anemia, Sickle Cell - therapy | Animals | Anemia, Sickle Cell - blood | Anemia, Sickle Cell - immunology | Care and treatment | Sickle cell anemia | Index Medicus | Isoimmunization | Reviews | Anemia | Blood transfusion | Erythrocytes
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6. Full Text Molecular epidemiological survey of haemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China
by Xiong, F and Sun, M and Zhang, X and Cai, R and Zhou, Y and Lou, J and Zeng, L and Sun, Q and Xiao, Q and Shang, X and Wei, X and Zhang, T and Chen, P and Xu, X
Clinical genetics, ISSN 0009-9163, 08/2010, Volume 78, Issue 2, pp. 139 - 148
molecular epidemiological survey | haemoglobinopathies | thalassaemia | Guangxi Zhuang Autonomous Region | Thalassaemia | Molecular epidemiological survey | Guangxi zhuang autonomous region | Haemoglobinopathies | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Hematologic and hematopoietic diseases | Anemias. Hemoglobinopathies | General aspects. Genetic counseling | Diseases of red blood cells | Medical genetics | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Geography | Prevalence | Humans | Molecular Sequence Data | Thalassemia - epidemiology | Male | China - epidemiology | Mutation - genetics | Health Surveys | DNA Mutational Analysis | Base Sequence | Hemoglobinopathies - diagnosis | Hemoglobins, Abnormal - genetics | Alleles | Hemoglobinopathies - genetics | Female | Heterozygote | Thalassemia - genetics | Hemoglobinopathies - epidemiology | Surveys | Hemoglobin | Medical colleges | Genetics | Epidemiology | Molecular biology | Index Medicus
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7. Full Text Wake-up Sleepy Gene: Reactivating Fetal Globin for β-Hemoglobinopathies
by Wienert, Beeke and Martyn, Gabriella E and Funnell, Alister P.W and Quinlan, Kate G.R and Crossley, Merlin
Trends in genetics, ISSN 0168-9525, 12/2018, Volume 34, Issue 12, pp. 927 - 940
genome editing | thalassemia | hemoglobinopathies | CRISPR-Cas9 | hereditary persistence of fetal hemoglobin | sickle cell disease | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | gamma-Globins - therapeutic use | Hemoglobinopathies - pathology | Humans | Hemoglobinopathies - blood | Genetic Therapy - trends | CRISPR-Cas Systems - genetics | beta-Globins - genetics | beta-Globins - therapeutic use | Hemoglobinopathies - genetics | Adult | gamma-Globins - genetics | Mutation | Gene Editing - trends | Index Medicus
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8. Full Text Rare hemoglobin variants in Tunisian population
by Zorai, A and Moumni, I and Mosbahi, I and Douzi, K and Chaouachi, D and Guemira, F and Abbes, S
International journal of laboratory hematology, ISSN 1751-5521, 04/2015, Volume 37, Issue 2, pp. 148 - 154
Tunisians | Hemoglobin variants | DNA sequencing | Life Sciences & Biomedicine | Hematology | Science & Technology | Humans | Erythrocyte Indices | Genotype | Hemoglobins - genetics | RNA Stability | beta-Globins - genetics | Genetic Variation | Phenotype | DNA Mutational Analysis | alpha-Globins - genetics | Hemoglobinopathies - diagnosis | Alleles | Hemoglobinopathies - genetics | Population Surveillance | delta-Globins - genetics | Amino Acid Substitution | Hemoglobinopathies - epidemiology | Tunisia - epidemiology | Hemoglobin | Index Medicus | Tunisia/epidemiology | Hemoglobinopathies/epidemiology | Hemoglobinopathies/genetics | delta-Globins/genetics | Hemoglobinopathies/diagnosis | alpha-Globins/genetics | Life Sciences | Human health and pathology | Hemoglobins/genetics | beta-Globins/genetics
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9. Full Text Fetal globin gene repressors as drug targets for molecular therapies to treat the β-globinopathies
by Suzuki, Mikiko and Yamamoto, Masayuki and Engel, James Douglas
Molecular and cellular biology, ISSN 0270-7306, 2014, Volume 34, Issue 19, pp. 3560 - 3569
Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Hemoglobinopathies - pathology | Humans | Gene Silencing | Repressor Proteins - genetics | Molecular Targeted Therapy | Hemoglobinopathies - drug therapy | Repressor Proteins - antagonists & inhibitors | Hemoglobinopathies - therapy | Transcription Factors - metabolism | Gene Expression Regulation, Developmental | Fetal Hemoglobin - genetics | Hemoglobinopathies - genetics | Mutation | Repressor Proteins - metabolism | Fetal Hemoglobin - metabolism | Index Medicus | Minireview
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