| 000 | 01561 a2200445 4500 | ||
|---|---|---|---|
| 005 | 20250516160444.0 | ||
| 264 | 0 | _c20150420 | |
| 008 | 201504s 0 0 eng d | ||
| 022 | _a1744-5094 | ||
| 024 | 7 |
_a10.3109/13816810.2013.811269 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aTarlan, Berçin | |
| 245 | 0 | 0 |
_aA case of 22q11.2 deletion syndrome with right microphthalmia and left corneal staphyloma. _h[electronic resource] |
| 260 |
_bOphthalmic genetics _cDec 2014 |
||
| 300 |
_a248-51 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 | _aAbnormalities, Multiple |
| 650 | 0 | 4 |
_aAphakia _xcongenital |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 22 _xgenetics |
| 650 | 0 | 4 | _aConsanguinity |
| 650 | 0 | 4 |
_aCorneal Diseases _xdiagnosis |
| 650 | 0 | 4 |
_aDevelopmental Disabilities _xdiagnosis |
| 650 | 0 | 4 |
_aDiGeorge Syndrome _xdiagnosis |
| 650 | 0 | 4 |
_aGrowth Disorders _xdiagnosis |
| 650 | 0 | 4 |
_aHeart Septal Defects, Ventricular _xdiagnosis |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aIn Situ Hybridization, Fluorescence |
| 650 | 0 | 4 |
_aKidney _xabnormalities |
| 650 | 0 | 4 | _aMagnetic Resonance Imaging |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMicrophthalmos _xdiagnosis |
| 700 | 1 | _aKiratli, Hayyam | |
| 700 | 1 | _aKılıç, Esra | |
| 700 | 1 | _aUtine, Eda | |
| 700 | 1 | _aBoduroğlu, Koray | |
| 773 | 0 |
_tOphthalmic genetics _gvol. 35 _gno. 4 _gp. 248-51 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.3109/13816810.2013.811269 _zAvailable from publisher's website |
| 999 |
_c22899266 _d22899266 |
||