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Affymetrix cytogenetics whole genome 2.7 M arrays were used for detecting the genomic DNA from the patient and the parents. An 88-kb duplication was identified at the chromosome 17: 67,024,087-67,112,435 region in the patient and the mother (black arrows). This result indicated that the change was a polymorphism and not a cause of 46,XX male disorder of sex development.
