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Tsezou, Aspasia; Kitsiou, Sofia; Galla, Angeliki; Petersen, Michael B.; Karadima, Georgia; Syrrou, Maria; Sahlèn, Sigrid; Blennow, Elisabeth
American journal of medical genetics, 13 March 2000, Letnik: 91, Številka: 2Journal Article
We report on two additional cases with duplication of 9p, minor with facial anomalies and developmental delay. Using fluorescence in situ hybridization and single‐copy probes, we showed that the first case was a direct duplication, whereas the second case was inverted. The extent of the direct duplication was defined as 9p12 → p24 by microdissection and microcloning of the aberrant chromosome and subsequent chromosome‐specific comparative genomic hybridization. DNA polymorphism analysis with eight microsatellite markers revealed that the origin of the dup(9p) was maternal in the first case, whereas it was paternal in the second. Am. J. Med. Genet. 91:102–106, 2000. © 2000 Wiley‐Liss, Inc.
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