000 01446 a2200421 4500
005 20250518075612.0
264 0 _c20200205
008 202002s 0 0 eng d
022 _a0065-2598
024 7 _a10.1007/978-3-030-27378-1_36
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aHabibi, Imen
245 0 0 _aMutations in VSX2, SOX2, and FOXE3 Identified in Patients with Micro-/Anophthalmia.
_h[electronic resource]
260 _bAdvances in experimental medicine and biology
_c2019
300 _a221-226 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAnophthalmos
_xgenetics
650 0 4 _aEgypt
650 0 4 _aForkhead Transcription Factors
_xgenetics
650 0 4 _aFrameshift Mutation
650 0 4 _aHomeodomain Proteins
_xgenetics
650 0 4 _aHumans
650 0 4 _aMicrophthalmos
_xgenetics
650 0 4 _aMutation
650 0 4 _aPhenotype
650 0 4 _aSOXB1 Transcription Factors
_xgenetics
650 0 4 _aSequence Deletion
650 0 4 _aTranscription Factors
_xgenetics
700 1 _aYoussef, Mohamed
700 1 _aMarzouk, Eman
700 1 _aEl Shakankiri, Nihal
700 1 _aGawdat, Ghada
700 1 _aEl Sada, Mohamed
700 1 _aF Schorderet, Daniel
700 1 _aAbou Zeid, Hana
773 0 _tAdvances in experimental medicine and biology
_gvol. 1185
_gp. 221-226
856 4 0 _uhttps://doi.org/10.1007/978-3-030-27378-1_36
_zAvailable from publisher's website
999 _c30467026
_d30467026