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Figure 1 | BMC Medical Genetics

Figure 1

From: Genome-wide sequencing for the identification of rearrangements associated with Tourette syndrome and obsessive-compulsive disorder

Figure 1

The 400 kb deletion carried by the proband. The deletion is mapped by SNP 6 array analysis and FISH hybridization on DNA and metaphase chromosomes, respectively. A. SNP 6 array data over the 6q-region showing the heterozygous deletion B. FISH using a BAC probe within the deletion hybridizes to the normal chromosome 6 but not to the chromosome 6 derivative.

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BMC Medical Genetics

ISSN: 1471-2350

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