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Fig. 3 | Molecular Cytogenetics

Fig. 3

From: Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?

Fig. 3

Results of expression analyses for a GARNL3, b RALGPS1, and c STXBP1. The mean expression of five unaffected controls is set to 1.0 (dark grey bar). The expression level of the patients (light grey) is set in relation to the mean of the five controls. Error bars are based on the data obtained over three experiments. Asterisks mark significant expression differences between patients and controls (p < 0.05, Wilcoxon-test)

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Molecular Cytogenetics

ISSN: 1755-8166