Characterization of copy number variation in genomic regions containing STR loci using array comparative genomic hybridization

Forensic Science International: Genetics

Volumn 7, Issue 5, 2013, Pages 475-481

  Repnikova, Elena A ^a   Rosenfeld, Jill A ^b   Bailes, Andrea ^a   Weber, Cecilia ^a   Erdman, Linda ^a   McKinney, Aimee ^a   Ramsey, Sarah ^a   Hashimoto, Sayaka ^a   Lamb Thrush, Devon ^a,c   Astbury, Caroline ^a   Reshmi, Shalini C ^a   Shaffer, Lisa G ^b,c   Gastier Foster, Julie M ^a,d   Pyatt, Robert E ^a,d  

^a NATIONWIDE CHILDREN S HOSPITAL   (United States)

^b PERKINELMER INC   (United States)

^c Paw Print Genetics Genetic Veterinary Sciences Inc   (United States)

^d THE OHIO STATE UNIVERSITY COLLEGE OF MEDICINE   (United States)

Author keywords

Array CGH; Copy number variation; Forensic analysis; Short tandem repeats

Indexed keywords

ARTICLE; CHROMOSOME 11; CHROMOSOME 12; CHROMOSOME 13; CHROMOSOME 16; CHROMOSOME 2; CHROMOSOME 21; CHROMOSOME 4; CHROMOSOME 7; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; COPY NUMBER VARIATION; FEMALE; HUMAN; MALE; PRIORITY JOURNAL; SHORT TANDEM REPEAT;

ARRAY CGH; COPY NUMBER VARIATION; FORENSIC ANALYSIS; SHORT TANDEM REPEATS;

AMELOGENIN; BONE MARROW TRANSPLANTATION; COMPARATIVE GENOMIC HYBRIDIZATION; DNA COPY NUMBER VARIATIONS; FEMALE; FORENSIC GENETICS; GENOME, HUMAN; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MICROSATELLITE REPEATS; PATERNITY;

EID: 84879626865     PISSN: 18724973     EISSN: 18780326     Source Type: Journal    
DOI: 10.1016/j.fsigen.2013.05.008     Document Type: Article

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