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Figure 1 | BMC Medical Genetics

Figure 1

From: Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: Relevance to ocular dysgenesis and hearing impairment

Figure 1

Schematic diagram of the distal tip of human chromosome 6p. The black boxes indicate regions where the patients are not deleted. White boxes indicate the minimum extent of the deletion. Grey boxes indicate the maximum extent of the deletion. Markers used are listed to the left of the patients chromosomes under locus. Genes in this region are listed in bold print. The genetic distance of markers, in Mb (megabases) from the telomere, are also indicated.

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