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Figure 1 | BMC Medical Genetics

Figure 1

From: A novel deletion mutation in the TUSC3 gene in a consanguineous Pakistani family with autosomal recessive nonsyndromic intellectual disability

Figure 1

Pedigree of a Pakistani family segregating AR-NSID. Square represent male and circles female while black symbols represents affected individuals and clear symbols unaffected individuals. Autozygosity mapping was done for individuals IV-11, IV-12, IV-13 and IV-14. All affected individuals share a homozygous haplotype in the chromosome 8p23.1 region, which is shown in boxes. Markers with physical map distances are shown on the left side.

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BMC Medical Genetics

ISSN: 1471-2350

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