High-throughput mutational screening for beta-thalassemia by single-nucleotide extension

Electrophoresis

Volumn 28, Issue 23, 2007, Pages 4289-4294

  Galbiati, Silvia ^a   Chiari, Marcella ^b   Macellari, Micol ^a   Ferrari, Maurizio ^a,c,d   Cremonesi, Laura ^a   Cretich, Marina ^b  

^a SAN RAFFAELE HOSPITAL   (Italy)

^b CNR   (Italy)

^c VITA SALUTE SAN RAFFAELE UNIVERSITY   (Italy)

^d Diagnostica e Ricerca San Raffaele SpA   (Italy)

Author keywords

Capillary array electrophoresis; DNA; Mutation detection

Indexed keywords

CAPILLARY ELECTROPHORESIS; DIAGNOSIS; DNA SEQUENCES; NUCLEOTIDES;

CAPILLARY ARRAY ELECTROPHORESIS; GLOBIN GENE; HIGH-THROUGHPUT; HIGH-THROUGHPUT METHOD; MEDITERRANEAN AREAS; MULTI-COLOR DETECTION; MUTATION DETECTION; NUMBER OF SAMPLES; SINGLE NUCLEOTIDES; THALASSAEMIA;

DNA;

ADENINE; BETA GLOBIN; CYTOSINE; GUANINE; HEMOGLOBIN C; HEMOGLOBIN S; TYROSINE;

AMINO ACID SUBSTITUTION; ARTICLE; BETA THALASSEMIA; CONTROLLED STUDY; DIAGNOSTIC PROCEDURE; DNA SEQUENCE; ELECTROPHORESIS; GENE MUTATION; GENETIC SCREENING; GENOTYPE; HIGH THROUGHPUT SCREENING; HUMAN; HUMAN CELL; MUTATIONAL ANALYSIS; PATHOGENESIS; POLYMERASE CHAIN REACTION; RELIABILITY; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; SOUTHERN EUROPE;

EID: 37149053122     PISSN: 01730835     EISSN: 15222683     Source Type: Journal    
DOI: 10.1002/elps.200700181     Document Type: Article

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