subject area of
- De novoβ-globin gene mutation [β63(E7)HIS→TYR] giving rise to Hb M disease in a newfoundlander Journal Articles
- Effect of Lead on Globin Synthesisin Vitro Journal Articles
- A Multicenter Trial of the Effectiveness of ζ-Globin Enzyme-Linked Immunosorbent Assay and Hemoglobin H Inclusion Body Screening for the Detection of α0-Thalassemia Trait Journal Articles
- A Novel Sickle Hemoglobin: Hemoglobin S-South End Journal Articles
- A Reliable Screening Test to Identify Adult Carriers of the (--SEA) alpha0-Thalassemia Deletion Journal Articles
- A T-to-G Transversion at Nucleotide −567 Upstream of HBG2 in a GATA-1 Binding Motif Is Associated with Elevated Hemoglobin F Journal Articles
- A novel monoclonal antibody based diagnostic test for alpha-thalassemia- 1 carriers due to the (-SEA/) deletion Journal Articles
- A rapid and simple electrophoretic method for the detection of mutations involving small insertion or deletion: application to ?-thalassemia Journal Articles
- Abnormal Haem Binding and Globin SH Group Blockade in Unstable Haemoglobins Journal Articles
- Access to a Syllabus of Human Hemoglobin Variants (1996) Via the World Wide Web Journal Articles
- Allelic Stability of VNTR Locus 3’αHVR: Linkage Disequilibrium with the Common α-Thalassaemia-1-Deletion of South-East Asia (--SEA/) Journal Articles
- Alpha-thalassaemia and population health in Southeast Asia Journal Articles
- An immunoassay to detect human embryonic epsilon globin chains by a murine monoclonal antibody Journal Articles
- Anti-ζ Antibody Screening for α-Thalassemia Using Dried Filter Paper Blood Journal Articles
- Carrier detection and prenatal diagnosis of hemoglobinopathies in Ontario. Journal Articles
- Characterisation of a novel 49·3 kb Gγ(Aγδβ)0‐thalassaemia deletion in seven families of Asian descent Journal Articles
- Characterization of a Rare Single α-Globin Gene Deletion in a Chinese Woman with Hb H Disease Journal Articles
- Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complex. Journal Articles
- Comparison of haemoglobin H inclusion bodies with embryonic zeta globin in screening for alpha thalassaemia. Journal Articles
- DOMINANT β-THALASSEMIA DUE TO A NEWLY IDENTIFIED FRAMESHIFT MUTATION IN EXON 3 (CODON 113, GTG → TG) Journal Articles
- De novo mutation of the β-globin gene initiation codon (ATG→AAG) in a Northern European Journal Articles
- Derivation and Characterization of Hematopoietic Cells From Human Embryonic Stem Cells Journal Articles
- Detection of Severe Nondeletionalα-Thalassemia Mutations Using a Single-Tube Multiplex ARMS Assay Journal Articles
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Detection of the (–
SEA ) double α‐globin gene deletion by a simple immunologic assay for embryonic ζ‐globin chains Journal Articles - Detection of α2- and α1- Globin Gene Variants by a Modified Cycle Sequencing Method Journal Articles
- Diagnostic Pitfall in PCR-Based α-Thalassemia Genotyping Resulting from a (G→C) Polymorphism at Nucleotide 71 3′ to the α2-Globin Gene Termination Codon Journal Articles
- Dominantly inherited β thalassaemia intermedia caused by a new single nucleotide deletion in exon 2 of the β globin gene: Hb morgantown (β91 CTG>CG) Journal Articles
- ERYTHROPOIETIN EFFECTS ON FETAL MOUSE ERYTHROID CELLS Journal Articles
- Elimination of Transfusions Through Induction of Fetal Hemoglobin Synthesis in Cooley's Anemiaa Journal Articles
- Embryonic and fetal globins are expressed in adult erythroid progenitor cells and in erythroid cell cultures Journal Articles
- Embryonic ζ-Globin Chains in Adults: a Marker for α-Thalassemia-1 Haplotype Due to a >17.5-kb Deletion Journal Articles
- Ethanol Inhibition of Haemoglobin Synthesis: In Vitro Evidence for a Haem Correctable Defect in Normal Subjects and in Alcoholics Journal Articles
- Expression of embryonic globins by erythroid cells in juvenile chronic myelocytic leukemia Journal Articles
- Expression of embryonic zeta-globin and epsilon-globin chains in a 10- year-old girl with congenital anemia Journal Articles
- Filipino ?-thalassemia due to a large deletion: identification of the deletion end points and polymerase chain reaction (PCR)-based diagnosis Journal Articles
- Frameshift Mutation in the α2-Globin Gene Causing α+-Thalassemia: Codon 49 (−GC) Journal Articles
- Globin Synthesis in Sideroblastic Anaemia I α AND β PEPTIDE CHAIN SYNTHESIS Journal Articles
- Hb Castilla [β32(B14)Leu → Arg] Caused by a De Novo Mutation Journal Articles
- Hb E/Hb LeporeHollandia in a family from Bangladesh Journal Articles
- Hb H hydrops foetalis syndrome: a case report and review of literature Journal Articles
- Hb S/β°‐Thalassemia due to the ˜1.4‐kb deletion is associated with a relatively mild phenotype Journal Articles
- HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server Journal Articles
- Hemoglobin Bart's Disease in an Italian Boy Journal Articles
- Hemoglobin Titusville, a low oxygen affinity variant hemoglobin, in a family of Northern European background Journal Articles
- Hemoglobin barts hydrops fetalis syndrome. Journal Articles
- Hemoglobin synthesis in siderocytes of flexed-tailed mutant (f/f) fetal mice Journal Articles
- Hemoglobinopathies mimicking Hb S/β‐thalassemia: Hb S/S with α‐thalassemia and Hb S/Volga Journal Articles
- High Oxygen Affinity Hemoglobin Variant in a Canadian Family: Hb Bunbury [β94(FG1)Asp→Asn,GAC→AAC] Journal Articles
- High hemoglobin A2 beta 0-thalassemia due to a 532-basepair deletion of the 5' beta-globin gene region. Journal Articles
- Homozygous HB Sallanches [α104(G11)CYS→TYR] in a Pakistani Child with HB H Disease Journal Articles
- Human embryonic zeta-globin chain expression in deletional alpha- thalassemias Journal Articles
- Human embryonic zeta-globin chains in adult patients with alpha-thalassemias. Journal Articles
- Human embryonic zeta-globin chains in fetal and newborn blood Journal Articles
- Human embryonic zeta-globin gene expression in mouse-human hybrid erythroid cell lines Journal Articles
- Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care Problem Journal Articles
- IDENTIFICATION OF TWO NEW α-THALASSEMIA MUTATIONS IN EXON 2 OF THE α1-GLOBIN GENE Journal Articles
- Identifican of A New High Oxygen Affinity Hemoglobin Variant: Hb Aurora [β139(H17)Asn→Tyr] Journal Articles
- Identification of a new hemoglobin variant: Hb St. Joseph's [β77(EF1)His→Leu] Journal Articles
- Identification of a novel termination codon mutation (TAA-->TAT, Term-- >Tyr) in the alpha 2 globin gene of a Laotian girl with hemoglobin H disease [letter] Journal Articles
- Identification of a novel β0 ‐ thalassaemia mutation in a greek family and subsequent prenatal diagnosis Journal Articles
- Identification of an extensive ζ‐α globin gene deletion in a Chinese individual Journal Articles
- Identification of two novel β°-thalassemia mutations in a filipino family: Frameshift codon 67 (− TG) and a β-globin gene deletion Journal Articles
- Increase in Hemoglobin Concentration during Therapy with Hydroxyurea in Cooley's Anemia Journal Articles
- Multiple Minisequencing Screen for Seven Southeast Asian Nondeletional α-Thalassemia Mutations Journal Articles
- NOVEL β-THALASSEMIA MUTATION IN A β-THALASSEMIA INTERMEDIA PATIENT [POLY A (AATAAA →GATAAA)] Journal Articles
- Nonisotopic Detection of Human Papillomavirus DNA in Clinical Specimens Using a Consensus PCR and a Generic Probe Mix in an Enzyme-Linked Immunosorbent Assay Format Journal Articles
- Novel Mutation of the α2-Globin Gene Initiation Codon (Atg→A-G) in a Vietnamese Girl with Hb H Disease Journal Articles
- Novel seventeen basepair deletion in exon 3 of the β-globin gene Journal Articles
- Novel β°-Thalassemia Mutation in a Canadian Woman of British Descent (Codons 72/73, -Agtga, +T) Journal Articles
- PCR-based diagnosis of the Filipino (??FIL) and Thai (??THAI) ?-thalassemia-1 deletions Journal Articles
- PROGRAM DESCRIPTION Journal Articles
- Peripheral Blood Gene Expression Changes during Allergen Inhalation Challenge in Atopic Asthmatic Individuals Journal Articles
- PhenCode: connecting ENCODE data with mutations and phenotype Journal Articles
- Positional effect of cis/trans alpha globin gene deletions on the formation of “H” bodies Journal Articles
- Prenatal exclusion of β thalassaemia major by examination of maternal plasma Journal Articles
- Prevalence of selective inhibition of HPV‐16 DNA amplification in cervicovaginal lavages Journal Articles
- Proportion of fetal hemoglobin synthesis decreases during erythroid cell maturation. Journal Articles
- Real-time PCR assays using internal controls for quantitation of HPV-16 and β-globin DNA in cervicovaginal lavages Journal Articles
- Routine Screening of (--<sup>SEA</sup>) α-Thalassemia Deletion by an Enzyme-Linked Immunosorbent Assay for Embryonic ζ-Globin Chains Journal Articles
- Second Report of Hb Toulon [α77(EF6)Pro→His] in a Canadian Family of Italian Descent Journal Articles
- Sequential Analysis of α‐ and β‐Globin Gene Expression During Erythropoietic Differentiation from Primate Embryonic Stem Cells Journal Articles
- Severity of β‐thalassemia due to genotypes involving the IVS‐I‐6 (T→C) mutation Journal Articles
- Should we screen for globin gene mutations in blood samples with mean corpuscular volume (MCV) greater than 80 fL in areas with a high prevalence of thalassaemia? Journal Articles
- Sickle cell disease caused by Hb S/Québec‐CHORI: Treatment with hydroxyurea and response Journal Articles
- Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7‐kb β‐globin gene deletion Journal Articles
- Sickle cell disease: no longer a single gene disorder Journal Articles
- Simple non-invasive prenatal detection of Hb Bart's disease by analysis of fetal erythrocytes in maternal blood Journal Articles
- Single-Tube Multiplex-PCR Screen for Anti-3.7 and Anti-4.2 α-Globin Gene Triplications Journal Articles
- Spectrum of β-Thalassemia Mutations in Egypt Journal Articles
- The Human Enhancer Blocker CTC-binding Factor Interacts with the Transcription Factor Kaiso Journal Articles
- The Interaction of Anti 3. 7 Type Quadruplicated α-Globin Genes and Heterozygous β-Thalassemia Journal Articles
- The T----C substitution at nucleotide + 1570 of the beta-globin gene is a polymorphism [letter; comment] Journal Articles
- The alpha-globin gene cluster: genetics and disorders. Journal Articles
- The effect of alpha-hemoglobin gene deletions on the red blood cells' mean cell volume and hemoglobin levels. Journal Articles
- Three New α-Thalassemia Point Mutations Ascertained Through Newborn Screening Journal Articles
- Three New β-Globin Gene Promoter Mutations Identified Through Newborn Screening Journal Articles
- Treatment of Two Infants with Cooley's Anemia with Sodium Phenylbutyrate Journal Articles
- Two novel beta-thalassemia mutations in the 5' and 3' noncoding regions of the beta-globin gene [see comments] Journal Articles
- Unequal α and β Globin mRNA in Reticulocytes of Normal and Mutant f/f Fetal Mice Journal Articles
- Universal Newborn Screening for Hb H Disease in California Journal Articles
- VEGF-A165 augments erythropoietic development from human embryonic stem cells Journal Articles
- α‐Thalassemia: Hb H Disease and Hb Barts Hydrops Fetalis Journal Articles
- β-Thalassemia intermedia in a lebanese child due to homozygosity for the -88 (C→T) Mutation Journal Articles
- β‐thalassemia intermedia caused by compound heterozygosity for Hb Malay (β codon 19 AAC→AGC; Asn→Ser) and codons 41/42 (‐CTTT) β 0 ‐thalassemia mutation Journal Articles
- β‐thalassemia intermedia due to compound heterozygosity for two β‐globin gene promoter mutations, including a novel TATA box deletion Journal Articles
- δβ-Thalassemia in an African-American: Identification of the deletion endpoints and PCR-Based diagnosis Journal Articles