<?xml version="1.0" encoding="ASCII"?>
<biogps><data><item><item key="factor_count">3</item><item key="sample_count">8</item><item key="tags"><item>chin</item><item>ectodermal dysplasia</item><item>nose</item><item>skin</item><item>syndrome</item></item><item key="slug">expression-data-from-skin-fibroblasts-derived-from</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-16524</item><item key="id">3313</item><item key="species">human</item><item key="name">Expression data from skin fibroblasts derived from Setleis Syndrome patients and normal controls</item></item><item><item key="factor_count">0</item><item key="sample_count">11</item><item key="tags"><item>cell</item><item>ectodermal dysplasia</item><item>protein</item><item>syndrome</item></item><item key="slug">transcription-profiling-of-human-cell-lines-from-h</item><item key="is_default">False</item><item key="geo_gse_id">E-GEOD-8646</item><item key="id">4981</item><item key="species">human</item><item key="name">Transcription profiling of human cell lines from Hay Wells Syndrome-Derived TAp63alphaQ540L mutant rveals impaired transcriptional and cell growth regulatory activity</item></item></data></biogps>
