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![]() Date: 2008-12-06 10:39:14Congenital disorders Rare diseases Skull Craniosynostosis Crouzon syndrome Apert syndrome Pfeiffer syndrome Muenke syndrome Carpenter syndrome Health Syndromes Genodermatoses | Source URL: www.ameriface.orgDownload Document from Source WebsiteFile Size: 125,39 KBShare Document on Facebook |
![]() | Brain phenotypes in two FGFR2 mouse models for Apert syndromeDocID: 1lqdu - View Document |
![]() | FGF/FGFR Signaling Coordinates Skull Development by Modulating Magnitude of Morphological Integration: Evidence from Apert Syndrome Mouse Models Neus Martı´nez-Abadı´as1, Yann Heuze´1, Yingli Wang2, Ethylin Wang JabDocID: 1krlW - View Document |
![]() | FGF/FGFR Signaling Coordinates Skull Development by Modulating Magnitude of Morphological Integration: Evidence from Apert Syndrome Mouse Models Neus Martı´nez-Abadı´as1, Yann Heuze´1, Yingli Wang2, Ethylin Wang JabDocID: 1gf6m - View Document |
![]() | Brain phenotypes in two FGFR2 mouse models for Apert syndromeDocID: 1fzZQ - View Document |
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