Diagnostic approach to hemoglobinopathies

Hemoglobin

Volumn 31, Issue 2, 2007, Pages 243-250

  Kutlar, Ferdane ^a  

^a MEDICAL COLLEGE OF GEORGIA   (United States)

Author keywords

DNA analysis; Hemoglobin (Hb) variants; Molecular diagnosis; Screening methods; Thalassemia(s)

Indexed keywords

2 PROPANOL; COMPLEMENTARY DNA; GENOMIC DNA; HEMOGLOBIN; NUCLEIC ACID; PROTEIN P50;

ALGORITHM; ANAMNESIS; BLOOD CELL COUNT; BLOOD EXAMINATION; CATION EXCHANGE; CONFERENCE PAPER; DIAGNOSTIC PROCEDURE; DNA SEQUENCE; ELECTROPHORESIS; ERYTHROCYTE; GENETIC VARIABILITY; HEMOGLOBIN SYNTHESIS; HEMOGLOBINOPATHY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; ISOELECTRIC FOCUSING; OXYGEN AFFINITY; PHENOTYPE; POLYMERASE CHAIN REACTION; RETICULOCYTE COUNT; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; THALASSEMIA;

AMINO ACID SUBSTITUTION; BASE SEQUENCE; DNA; HEMOGLOBINOPATHIES; HEMOGLOBINS; HEMOGLOBINS, ABNORMAL; HUMANS; MOLECULAR SEQUENCE DATA; POLYMORPHISM, SINGLE NUCLEOTIDE; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; THALASSEMIA; VARIATION (GENETICS);

EID: 34248186004     PISSN: 03630269     EISSN: 1532432X     Source Type: Journal    
DOI: 10.1080/03630260701297071     Document Type: Conference Paper

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