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Postzygotic telomere capture causes segmental UPD, duplication and deletion of chromosome 8p in a patient with intellectual disability and obesity.
Inside the 8p23.1 duplication syndrome; eight microduplications of likely or uncertain clinical significance.
Inverted duplication deletion of 8P: characterization by standard cytogenetic and SNP array analyses.
8p23.1 duplication syndrome; common, confirmed, and novel features in six further patients.
[Cytogenetic and molecular genetic study of a case with 8p inverted duplication deletion syndrome].