Carrier detection in Duchenne and Becker muscular dystrophy using dinucleotide repeat polymorphisms. A study in Mexican families

Archives of Medical Research

Volumn 27, Issue 2, 1996, Pages 151-156

  Arenas, D ^a   Coral, R ^a   Cisneros, B ^a   Penaloza, L ^a   Salamanca, F ^a   Kofman, S ^a   Mercado, R ^a   Mendez, J ^a   Martinez, C ^a   Montanez, C ^a  

^a DEPARTAMENTO DE FÍSICA   (Mexico)

Author keywords

Carrier detection; DMD; PCR

Indexed keywords

DINUCLEOTIDE; DYSTROPHIN;

AMINO TERMINAL SEQUENCE; ARTICLE; BECKER MUSCULAR DYSTROPHY; CARBOXY TERMINAL SEQUENCE; DUCHENNE MUSCULAR DYSTROPHY; FEMALE; GENETIC POLYMORPHISM; GENETIC RECOMBINATION; HAPLOTYPE; HETEROZYGOTE DETECTION; HUMAN; INTRON; MAJOR CLINICAL STUDY; MEXICO; MOSAICISM;

HETEROZYGOTE DETECTION; HUMANS; MALE; MEXICO; MUSCULAR DYSTROPHIES; PEDIGREE; POLYMORPHISM, GENETIC; REPETITIVE SEQUENCES, NUCLEIC ACID;

EID: 0029890307     PISSN: 01880128     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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