000 01617 a2200553 4500
005 20250518044450.0
264 0 _c20200403
008 202004s 0 0 eng d
022 _a1744-5094
024 7 _a10.1080/13816810.2019.1622023
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aChapi, Marjan
245 0 0 _aIncomplete penetrance of
_h[electronic resource]
260 _bOphthalmic genetics
_c06 2019
300 _a259-266 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aCone-Rod Dystrophies
_xgenetics
650 0 4 _aFemale
650 0 4 _aGenes, Dominant
650 0 4 _aHomeodomain Proteins
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aPedigree
650 0 4 _aPenetrance
650 0 4 _aPhenotype
650 0 4 _aPolymorphism, Single Nucleotide
650 0 4 _aTrans-Activators
_xgenetics
650 0 4 _aVisual Acuity
650 0 4 _aExome Sequencing
650 0 4 _aYoung Adult
700 1 _aSabbaghi, Hamideh
700 1 _aSuri, Fatemeh
700 1 _aAlehabib, Elham
700 1 _aRahimi-Aliabadi, Simin
700 1 _aJamali, Faezeh
700 1 _aJamshidi, Javad
700 1 _aEmamalizadeh, Babak
700 1 _aDarvish, Hossein
700 1 _aMirrahimi, Mehraban
700 1 _aAhmadieh, Hamid
700 1 _aDaftarian, Narsis
773 0 _tOphthalmic genetics
_gvol. 40
_gno. 3
_gp. 259-266
856 4 0 _uhttps://doi.org/10.1080/13816810.2019.1622023
_zAvailable from publisher's website
999 _c29814691
_d29814691