Molecular and clinical characterization of a recurrent cryptic unbalanced t(4q;18q) resulting in an 18q deletion and 4q duplication

American Journal of Medical Genetics, Part A

Volumn 146, Issue 22, 2008, Pages 2898-2904

  Horbinski, Craig ^a   Carter, Erika M ^b   Heard, Patricia L ^b   Sathanoori, Malini ^c   Hu, Jie ^c   Vockley, Jerry ^d   Gunn, Shelly ^b   Hale, Daniel E ^b   Surti, Urvashi ^a   Cody, Jannine D ^b,e  

^a UNIVERSITY OF PITTSBURGH MEDICAL CENTER   (United States)

^b Mays Cancer Center at UT Health San Antonio   (United States)

^c UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

^d CHILDREN S HOSPITAL OF PITTSBURGH   (United States)

^e UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER AT SAN ANTONIO   (United States)

Author keywords

18q deletion; Array CGH; Chromosome 18; Chromosome 4; Cryptic translocation; Fluorescence in situ hybridization (FISH); Recurrent translocation

Indexed keywords

DNA;

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 18Q; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME TRANSLOCATION; COMPARATIVE GENOMIC HYBRIDIZATION; CYTOGENETICS; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; PRIORITY JOURNAL; REAL TIME POLYMERASE CHAIN REACTION;

ABNORMALITIES, MULTIPLE; ANEUPLOIDY; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 18; CHROMOSOMES, HUMAN, PAIR 4; COMPARATIVE GENOMIC HYBRIDIZATION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; PHENOTYPE; TRANSLOCATION, GENETIC;

ROBERTSONIA;

EID: 56049103585     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32557     Document Type: Article

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