Biomolecular identification of (CCTG)n mutation in myotonic dystrophy type 2 (DM2) by FISH on muscle biopsy.

European journal of histochemistry : EJH

Volumn 48, Issue 4, 2004, Pages 437-442

  Cardani, R ^a   Mancinelli, E ^a   Sansone, V ^a   Rotondo, G ^a   Meola, G ^a  

^a UNIVERSITY OF MILAN   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

REPETITIVE DNA;

ADULT; AGED; ARTICLE; BIOPSY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; HUMAN; MALE; MIDDLE AGED; MOLECULAR GENETICS; MOLECULAR PROBE; MYOTONIC DYSTROPHY; NUCLEOTIDE SEQUENCE; PATHOLOGY; SKELETAL MUSCLE;

ADULT; AGED; BASE SEQUENCE; BIOPSY; DNA REPEAT EXPANSION; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MIDDLE AGED; MOLECULAR PROBES; MOLECULAR SEQUENCE DATA; MUSCLE, SKELETAL; MYOTONIC DYSTROPHY;

MLCS; MLOWN;

EID: 21744451671     PISSN: 1121760X     EISSN: None     Source Type: Journal    
DOI: 10.4081/918     Document Type: Article

References (0)