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Keywords: 22q11.2 deletion syndromeClose
Development (2020) 147 (3): dev185256.
Published: 3 February 2020
..., in a distribution established in the early embryo. We further show that biallelic expression of the CPM regulatory gene Tbx1 , haploinsufficient in 22q11.2 deletion syndrome patients, is required for the correct patterning of muscles with CPM-derived connective tissue. Our results suggest that CPM plays...
Includes: Supplementary data
Development (2004) 131 (21): 5491–5502.
Published: 1 November 2004
... with del22q11. † Author for correspondence (e-mail: email@example.com ) * These authors contributed equally to this work 13 8 2004 © 2004. 2004 Tbx1 22q11.2 deletion syndrome Anterior heart field Foxa2 Fgf8 Fgf10 Human chromosomal deletion...