Unexpected detection of dystrophin gene deletions by array comparative genomic hybridization

American Journal of Medical Genetics, Part A

Volumn 152, Issue 9, 2010, Pages 2301-2307

  Cottrell, Catherine E ^a   Prior, Thomas W ^b   Pyatt, Robert ^a,b   Astbury, Caroline ^a,b   Reshmi, Shalini ^a,b   Bartholomew, Dennis ^a,b   Atkin, Joan ^a,b   Manickam, Kandamurugu ^a,b   Thrush, Devon Lamb ^a,b   Pastore, Matthew ^a,b   Mendell, Jerry ^a,b   Tsao, Chang Yong ^a,b   Al Dahhak, Roula ^a,b   Newmeyer, Amy ^a,b   Gastier Foster, Julie M ^a,b  

^a NATIONWIDE CHILDREN S HOSPITAL   (United States)

^b OHIO STATE UNIVERSITY   (United States)

Author keywords

Array comparative genomic hybridization; BMD; DMD; Dystrophin gene; Microarray; Muscular dystrophy

Indexed keywords

DYSTROPHIN;

ARTICLE; BECKER MUSCULAR DYSTROPHY; CASE REPORT; CHILD; COMPARATIVE GENOMIC HYBRIDIZATION; DNA MICROARRAY; DUCHENNE MUSCULAR DYSTROPHY; FEMALE; GENE DELETION; GENETIC COUNSELING; HUMAN; INHERITANCE; MALE; NEWBORN; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL;

AGE OF ONSET; CHILD, PRESCHOOL; COMPARATIVE GENOMIC HYBRIDIZATION; DYSTROPHIN; FAMILY; FEMALE; GENE DELETION; GENETIC COUNSELING; GENETIC TESTING; HUMANS; INFANT; INFANT, NEWBORN; MALE; MUSCULAR DYSTROPHY, DUCHENNE;

EID: 77956126310     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33532     Document Type: Article

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