Skip to main content
Fig. 2 | BMC Medical Genomics

Fig. 2

From: Pigmentary mosaicism as a recurrent clinical manifestation in three new patients with mosaic trisomy 12 diagnosed postnatally: cases report and literature review

Fig. 2

Cytogenomic analysis. (A) karyotype in DS of patient 1 showing only trisomy 12 cell line; (B) Patient 3 aCGH 400 K analysis showing chromosome 12 mosaic duplication (30%) in DS: arr[GRCh37] 12p13.33q24.33(64620_133201316) × 2 ~ 3 and (C) SNParray 750 K discarding copy number variants and UPD12 in PB of three patients

Back to article page