Identification of a rare de novo three-way complex t(5;20;8)(q31;p11.2;p21) with microdeletions on 5q31.2, 5q31.3, and 8p23.2 in a patient with hearing loss and global developmental delay: Case report

Molecular Cytogenetics

Volumn 2, Issue 1, 2009, Pages

  Haj, Roland ^a   Jackson, Kelly ^b   Torchia, Beth A ^a   Shaffer, Lisa G ^a   Bejjani, Bassem A ^a   Gowans, Gordon C ^b   Ruff, Michael W ^c  

^a PerkinElmer   (United States)

^b University of Louisville School of Medicine   (United States)

^c Jasper Pediatric Associates   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 5Q; CHROMOSOME 8P; CHROMOSOME ABERRATION; CHROMOSOME BAND; CHROMOSOME DELETION 5; CHROMOSOME IDENTIFICATION; CHROMOSOME TRANSLOCATION; CYTOGENETICS; DEVELOPMENTAL STAGE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HEARING IMPAIRMENT; HEARING LOSS; HUMAN; INFANT; KARYOTYPE; MICROARRAY ANALYSIS; MYOPATHY; PHYSICAL EXAMINATION; PRIORITY JOURNAL;

EID: 63449107896     PISSN: None     EISSN: 17558166     Source Type: Journal    
DOI: 10.1186/1755-8166-2-2     Document Type: Article

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