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An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome.
Frank DU, Fotheringham LK, Brewer JA, Muglia LJ, Tristani-Firouzi M, Capecchi MR, Moon AM. Frank DU, et al. Among authors: moon am. Development. 2002 Oct;129(19):4591-603. doi: 10.1242/dev.129.19.4591. Development. 2002. PMID: 12223415 Free PMC article.
699 results