000 01580 a2200481 4500
005 20250513035358.0
264 0 _c19951005
008 199510s 0 0 eng d
022 _a0964-6906
024 7 _a10.1093/hmg/4.6.1077
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aOldridge, M
245 0 0 _aMutations in the third immunoglobulin domain of the fibroblast growth factor receptor-2 gene in Crouzon syndrome.
_h[electronic resource]
260 _bHuman molecular genetics
_cJun 1995
300 _a1077-82 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAmino Acid Sequence
650 0 4 _aBase Sequence
650 0 4 _aCraniofacial Dysostosis
_xgenetics
650 0 4 _aDNA
650 0 4 _aDNA Mutational Analysis
650 0 4 _aExons
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMolecular Sequence Data
650 0 4 _aMutation
650 0 4 _aReceptor Protein-Tyrosine Kinases
_xgenetics
650 0 4 _aReceptor, Fibroblast Growth Factor, Type 2
650 0 4 _aReceptors, Fibroblast Growth Factor
_xgenetics
650 0 4 _aSequence Homology, Amino Acid
700 1 _aWilkie, A O
700 1 _aSlaney, S F
700 1 _aPoole, M D
700 1 _aPulleyn, L J
700 1 _aRutland, P
700 1 _aHockley, A D
700 1 _aWake, M J
700 1 _aGoldin, J H
700 1 _aWinter, R M
773 0 _tHuman molecular genetics
_gvol. 4
_gno. 6
_gp. 1077-82
856 4 0 _uhttps://doi.org/10.1093/hmg/4.6.1077
_zAvailable from publisher's website
999 _c7654893
_d7654893