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| First Page | Document Content | |
|---|---|---|
 Date: 2012-06-06 07:06:21Genetic genealogy Medical genetics Popliteal pterygium syndrome EUROCAT DiGeorge syndrome Apert syndrome Noonan syndrome Klippel–Feil syndrome Turner syndrome Health Syndromes Genodermatoses |
| 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 |