Fig. 1 | Genetics in Medicine

Fig. 1

From: A diagnostic approach to identifying submicroscopic 7p21 deletions in Saethre-Chotzen syndrome: Fluorescence in situ hybridization and dosage-sensitive Southern blot analysis

Fig. 1

A: Patient 4's partial composite karyotype shows the four derivative chromosomes with their normal homologues. B: Schematic representation of patient 4's derivative chromosomes, indicating the translocation breakpoints by horizontal bars. The band assignment is given on the respective normal homologues.

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