000 01307 a2200361 4500
005 20250516004707.0
264 0 _c20110531
008 201105s 0 0 eng d
022 _a1476-5438
024 7 _a10.1038/ejhg.2010.163
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aWeisschuh, Nicole
245 0 0 _aClinical utility gene card for: Axenfeld-Rieger syndrome.
_h[electronic resource]
260 _bEuropean journal of human genetics : EJHG
_cMar 2011
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAnterior Eye Segment
_xabnormalities
650 0 4 _aEye Abnormalities
_xdiagnosis
650 0 4 _aEye Diseases, Hereditary
650 0 4 _aForkhead Transcription Factors
_xgenetics
650 0 4 _aGenetic Testing
650 0 4 _aHomeodomain Proteins
_xgenetics
650 0 4 _aHumans
650 0 4 _aPrenatal Diagnosis
650 0 4 _aRisk Assessment
650 0 4 _aSensitivity and Specificity
650 0 4 _aTranscription Factors
_xgenetics
650 0 4 _aHomeobox Protein PITX2
700 1 _aDe Baere, Elfride
700 1 _aWissinger, Bernd
700 1 _aTümer, Zeynep
773 0 _tEuropean journal of human genetics : EJHG
_gvol. 19
_gno. 3
856 4 0 _uhttps://doi.org/10.1038/ejhg.2010.163
_zAvailable from publisher's website
999 _c20244519
_d20244519