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Coincidence between fragile site expression and interstitial deletion of chromosome 11 in a case of myelofibrosis

✍ Scribed by M. Sessarego; F. Ajmar; R. Ravazzolo; G. L. Bianchi Scarrà; C. Garrè; P. Boccaccio

Book ID: 104704580
Publisher: Springer
Year: 1983
Tongue: English
Weight: 264 KB
Volume: 63
Category: Article
ISSN: 0340-6717
DOI: 10.1007/bf00284671

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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