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Full record GDS3172

Treacher Collins Syndrome gene heterozygous mutation effect on embryos

Analysis of embryos heterozygous mutant for the Treacher Collins Syndrome (TCS) gene (TCOF1). TCS is a congenital disorder of craniofacial development arising from mutations in TCOF1. Results provide insight into the molecular pathogenesis of TCS.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 2 genotype/variation sets
Platform:
GPL1261
Series:
GSE10167
6 Samples
Download data: CEL, CHP, EXP
DataSet
Accession:
GDS3172
ID:
3172

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