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One or more keywords matched the following properties of Crkl deficiency disrupts Fgf8 signaling in a mouse model of 22q11 deletion syndromes.
PropertyValue
has major subject area list Chromosomes, Human, Pair 22; DiGeorge Syndrome; Fibroblast Growth Factor 8; Gene Deletion; Proto-Oncogene Proteins c-crk; Signal Transduction
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  • Velocardiofacial Syndrome