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Sequential FISH reveals an abnormal karyotype involving 14 chromosomes in a child with acute lymphoblastic leukemia

✍ Scribed by Pinson, M P; Martineau, M; Jabbar, M S; Kilby, A M; Walker, H; Harrison, C J

Book ID: 110054658
Publisher: Nature Publishing Group
Year: 2000
Tongue: English
Weight: 143 KB
Volume: 14
Category: Article
ISSN: 0887-6924
DOI: 10.1038/sj.leu.2401884

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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