Diagnosis of Duchenne/Becker muscular dystrophy and quantitative identification of carrier status by use of entangled solution capillary electrophoresis

Clinical Chemistry

Volumn 43, Issue 5, 1997, Pages 745-751

  Fortina, Paolo ^a,c   Cheng, Jing ^b   Shoffner, Mann A ^b   Surrey, Saul ^a   Hitchcock, Wendy M ^c   Kricka, Larry J ^b   Wilding, Peter ^b  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

^c CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

Author keywords

heritable disorders; laser induced fluorescence detection; polymerase chain reaction

Indexed keywords

DNA; DYSTROPHIN;

ARTICLE; BECKER MUSCULAR DYSTROPHY; CAPILLARY ELECTROPHORESIS; CONTROLLED STUDY; DUCHENNE MUSCULAR DYSTROPHY; FEMALE; FLUORESCENCE; GENE DOSAGE; HETEROZYGOTE; HUMAN; HUMAN CELL; LEUKOCYTE; MALE; POLYMERASE CHAIN REACTION; QUANTITATIVE DIAGNOSIS;

EID: 0030939302     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: 10.1093/clinchem/43.5.745     Document Type: Article

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