000 01098 a2200325 4500
005 20250515095016.0
264 0 _c20080328
008 200803s 0 0 eng d
022 _a1750-1172
024 7 _a10.1186/1750-1172-2-47
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aVerma, Amit S
245 0 0 _aAnophthalmia and microphthalmia.
_h[electronic resource]
260 _bOrphanet journal of rare diseases
_cNov 2007
300 _a47 p.
_bdigital
500 _aPublication Type: Journal Article; Review
650 0 4 _aAnophthalmos
_xembryology
650 0 4 _aHMGB Proteins
_xgenetics
650 0 4 _aHumans
650 0 4 _aMagnetic Resonance Imaging
650 0 4 _aMicrophthalmos
_xembryology
650 0 4 _aMutation
650 0 4 _aPrevalence
650 0 4 _aSOXB1 Transcription Factors
650 0 4 _aTranscription Factors
_xgenetics
650 0 4 _aVitamin A Deficiency
_xcomplications
700 1 _aFitzpatrick, David R
773 0 _tOrphanet journal of rare diseases
_gvol. 2
_gp. 47
856 4 0 _uhttps://doi.org/10.1186/1750-1172-2-47
_zAvailable from publisher's website
999 _c17554604
_d17554604