Original language | English |
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Pages (from-to) | 223 - 224 |
Number of pages | 2 |
Journal | Developmental Biology |
Volume | 356 |
Issue number | 1 |
DOIs | |
Publication status | Published - 2011 |
Sprouty loss of function mutations in the mouse results in defects characteristic of 22q11 deletion syndrome, which are exacerbated by Tbx1 haploinsufficiency
Subreena Simrick, Dorota Szumska, Jennifer Gardiner, Sagar Karun, Bernice Morrow, Shoumo Bhattacharya, Michiel A. Basson
Research output: Contribution to journal › Meeting abstract