| Literature DB >> 10602115 |
P Guanciali Franchi1, G Calabrese, E Morizio, E Modestini, L Stuppia, R Mingarelli, G Palka.
Abstract
Authors report on a case of partial 9p duplication, involving the 9p22-9p24 region. This represents the second case of such duplication in which the breakpoints were precisely defined using fluorescence in situ hybridisation (FISH) with chromosome 9 specific painting and YAC DNA probes, localised onto 9p22-9p24 region. FISH analysis pinpointed chromosome breakpoints in dup(9)(p22p24) and excluded an insertion or a translocation from other chromosomes. The present report supports the segment 9p22-9p24 as the critical region for the observed phenotype of the duplication 9p syndrome. Copyright 2000 Wiley-Liss, Inc.Mesh:
Year: 2000 PMID: 10602115
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299