Skip to main content
Figure 2 | BMC Medical Genetics

Figure 2

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

Figure 2

Linkage analysis. A) Multipoint genome-wide LOD scores. Linkage was calculated in MERLIN using family members marked with "+" on Figure 1, under a fully penetrant dominant model. Horizontal line marks LOD = 3.0. Arrow indicates linkage peak on chromosome 1p. B) Multipoint LOD scores on chromosome 1. The peak extends from SNP rs966321 to rs1441834 (8.0-56.7 cM), Max LOD = 2.41.

Back to article page

BMC Medical Genetics

ISSN: 1471-2350

Contact us