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 journalMeeting abstract

Original languageEnglish
Pages (from-to)223 - 224
Number of pages2
JournalDevelopmental Biology
Volume356
Issue number1
DOIs
Publication statusPublished - 2011

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