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T-cell acute lymphoblastic leukemia with add(1)(p36) and del(12)(p11) following acute myelocytic leukemia with partial deletion of 9p

✍ Scribed by Chikashi Yoshida; Kazumi Suzukawa; Yukitaka Katsura; Seiichi Shimizu; Harumi Y Mukai; Yuichi Hasegawa; Shigehiko Imagawa; Hiroshi Kojima; Toshiro Nagasawa


Book ID
113512302
Publisher
Elsevier Science
Year
2004
Tongue
English
Weight
196 KB
Volume
150
Category
Article
ISSN
0165-4608

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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