Fig. 3 | Genetics in Medicine

Fig. 3

From: Genotype–phenotype correlation in Smith-Magenis syndrome: Evidence that multiple genes in 17p11.2 contribute to the clinical spectrum

Fig. 3

Histograms representing significant phenotypic differences between RAI1 and 17p11.2 deletion cases: 17p11.2 deletion data (gray bar) and RAI1 mutation data (white bar). Proportions were compared using the Fisher exact test. P values are two-tailed. P values less than .05 are significant, and 95% confidence levels for the two groups are indicated. Also refer to Table 3.

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