000 01452 a2200385 4500
005 20250516034537.0
264 0 _c20111027
008 201110s 0 0 eng d
022 _a1542-0760
024 7 _a10.1002/bdra.20811
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aPurushothaman, Roopa
245 0 0 _aFacial suture synostosis of newborn Fgfr1(P250R/+) and Fgfr2(S252W/+) mouse models of Pfeiffer and Apert syndromes.
_h[electronic resource]
260 _bBirth defects research. Part A, Clinical and molecular teratology
_cJul 2011
300 _a603-9 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAcrocephalosyndactylia
_xgenetics
650 0 4 _aAnimals
650 0 4 _aCraniosynostoses
_xgenetics
650 0 4 _aDisease Models, Animal
650 0 4 _aFace
_xpathology
650 0 4 _aFemale
650 0 4 _aMale
650 0 4 _aMaxilla
_xpathology
650 0 4 _aMice
650 0 4 _aOsteogenesis
650 0 4 _aReceptor, Fibroblast Growth Factor, Type 1
_xgenetics
650 0 4 _aReceptor, Fibroblast Growth Factor, Type 2
_xgenetics
650 0 4 _aSkull Base
_xpathology
700 1 _aCox, Timothy C
700 1 _aMaga, A Murat
700 1 _aCunningham, Michael L
773 0 _tBirth defects research. Part A, Clinical and molecular teratology
_gvol. 91
_gno. 7
_gp. 603-9
856 4 0 _uhttps://doi.org/10.1002/bdra.20811
_zAvailable from publisher's website
999 _c20802817
_d20802817