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A new nonrandom chromosomal abnormality, t(2;16)(p11.2;p11.2), possibly associated with poor outcome in childhood acute lymphoblastic leukemia

✍ Scribed by Lisa R. Lowe; Nyla A. Heerema; Alexandra C. Cheerva; Catherine G. Palmer

Book ID: 119105530
Publisher: Elsevier Science
Year: 1992
Tongue: English
Weight: 388 KB
Volume: 64
Category: Article
ISSN: 0165-4608
DOI: 10.1016/0165-4608(92)90324-2

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## Abstract Greig cephalopolysyndactyly (GCPS; OMIM 175700) is an autosomal dominant condition caused by mutations of the gene __GLI3__, located on 7p13. To date, several cases of deletions and/or translocations involving this locus have been reported in patients with GCPS. __GLI3__ is a transcript