Detection of mutations in the dystrophin gene via automated DHPLC screening and direct sequencing

BMC Genetics

Volumn 2, Issue , 2001, Pages

  Bennett, Richard R ^a   den Dunnen, Johan ^b   O'Brien, Kristine F ^c   Darras, Basil T ^a   Kunkel, Louis M ^a,c  

^a BOSTON CHILDREN S HOSPITAL   (United States)

^b LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^c HARVARD MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DYSTROPHIN; GENOMIC DNA;

AMPLICON; ARTICLE; AUTOMATION; CLINICAL ARTICLE; CLINICAL LABORATORY; CONTROLLED STUDY; COST EFFECTIVENESS ANALYSIS; DENATURING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; DNA POLYMORPHISM; DUCHENNE MUSCULAR DYSTROPHY; FEMALE; GENE DELETION; GENE DUPLICATION; GENE MUTATION; GENE REARRANGEMENT; GENE SEQUENCE; HUMAN; MALE; NUCLEOTIDE SEQUENCE; POINT MUTATION;

EID: 2942523954     PISSN: 14712156     EISSN: None     Source Type: Journal    
DOI: 10.1186/1471-2156-2-17     Document Type: Article

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