000 01383 a2200433 4500
005 20250515092719.0
264 0 _c20071210
008 200712s 0 0 eng d
022 _a0022-1333
024 7 _a10.1007/s12041-007-0021-z
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aNallathambi, Jeyabalan
245 0 0 _aFOXL2 mutations in Indian families with blepharophimosis-ptosis-epicanthus inversus syndrome.
_h[electronic resource]
260 _bJournal of genetics
_cAug 2007
300 _a165-8 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aBlepharophimosis
_xcomplications
650 0 4 _aChild, Preschool
650 0 4 _aDNA Mutational Analysis
650 0 4 _aEye Diseases
_xcongenital
650 0 4 _aFamily
650 0 4 _aFemale
650 0 4 _aForkhead Box Protein L2
650 0 4 _aForkhead Transcription Factors
_xgenetics
650 0 4 _aHumans
650 0 4 _aIndia
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aPedigree
650 0 4 _aSyndrome
700 1 _aNeethirajan, Guruswamy
700 1 _aUsha, Kim
700 1 _aJitendra, Jethani
700 1 _aDe Baere, Elfride
700 1 _aSundaresan, Periasamy
773 0 _tJournal of genetics
_gvol. 86
_gno. 2
_gp. 165-8
856 4 0 _uhttps://doi.org/10.1007/s12041-007-0021-z
_zAvailable from publisher's website
999 _c17486993
_d17486993