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Figure 1 | BMC Medical Genetics

Figure 1

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

Figure 1

Pedigree drawing showing haplotypes on chromosome 1p for genotyped family members. The segregating haplotype is coloured black. All other haplotypes are white. Examined unaffected individuals are marked "N". Grey symbols indicate "unexamined but reportedly affected" individuals. The proband IV:5 is marked by an arrow. A "+" symbol indicates those included in the genome-wide scan. Recombinant individuals III:2 and IV:8 define the critical region between markers rs966321 and rs1441834.

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BMC Medical Genetics

ISSN: 1471-2350

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