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Figure 3 | BMC Medical Genetics

Figure 3

From: A novel syndrome of paediatric cataract, dysmorphism, ectodermal features, and developmental delay in Australian Aboriginal family maps to 1p35.3-p36.32

Figure 3

Phased haplotypes for all genotyped members of the family. Affected individuals and the segregating haplotype are shaded grey. Participants of uncertain diagnosis and carrier status are marked in bold. Both III:5 and III:6 clearly carry the segregating disease haplotype while IV:6 likely does not. Unaffected individuals IV:1, IV:3 and IV:9 do not carry this haplotype. "?" indicates allele not scored.

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BMC Medical Genetics

ISSN: 1471-2350

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