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Fig. 2 | BMC Medical Genetics

Fig. 2

From: A case report of primary ciliary dyskinesia, laterality defects and developmental delay caused by the co-existence of a single gene and chromosome disorder

Fig. 2

Array comparative genomic hybridisation. Array CGH was undertaken for patient V:1 on account of his developmental delay. a Image from Cytogenomics v2.7.22 software (Agilent) showing a ~1.6 Mb gain on 17q12 (hg19; chr17:34,611,352-36,248,918). b Screenshot from UCSC hg19 showing the 17 genes (UCSC) located within the duplicated region

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BMC Medical Genetics

ISSN: 1471-2350

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