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![]() Date: 2010-09-15 09:40:55Skull Syndromes Congenital disorders Head and neck Skeletal system Craniosynostosis Craniofacial surgery Brachycephaly Apert syndrome Health Anatomy Human anatomy | Add to Reading List |
![]() | 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 |
![]() | DEVELOPMENTAL DYNAMICS 239:3058–3071, 2010 a PATTERNS & PHENOTYPESDocID: 1fsy4 - View Document |