000 01173 a2200349 4500
005 20250514020216.0
264 0 _c20020206
008 200202s 0 0 eng d
022 _a0720-048X
024 7 _a10.1016/s0720-048x(01)00401-6
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aVanhoenacker, F M
245 0 0 _aHereditary multiple exostoses: from genetics to clinical syndrome and complications.
_h[electronic resource]
260 _bEuropean journal of radiology
_cDec 2001
300 _a208-17 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aChromosome Mapping
650 0 4 _aChromosomes, Human, Pair 11
650 0 4 _aExostoses, Multiple Hereditary
_xcomplications
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aMagnetic Resonance Imaging
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aRetrospective Studies
700 1 _aVan Hul, W
700 1 _aWuyts, W
700 1 _aWillems, P J
700 1 _aDe Schepper, A M
773 0 _tEuropean journal of radiology
_gvol. 40
_gno. 3
_gp. 208-17
856 4 0 _uhttps://doi.org/10.1016/s0720-048x(01)00401-6
_zAvailable from publisher's website
999 _c11644981
_d11644981