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Cytogenetic analysis of primary neuroblastoma with del(1), del(14), hsr, and dmin chromosomes

✍ Scribed by Iskra Petković; Mladen Čepulić


Book ID
119104866
Publisher
Elsevier Science
Year
1991
Tongue
English
Weight
214 KB
Volume
55
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