| 000 | 01474 a2200457 4500 | ||
|---|---|---|---|
| 005 | 20250513092518.0 | ||
| 264 | 0 | _c19960822 | |
| 008 | 199608s 0 0 eng d | ||
| 022 | _a0161-6420 | ||
| 024 | 7 |
_a10.1016/s0161-6420(96)30563-0 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aChen, R M | |
| 245 | 0 | 0 |
_aOphthalmic manifestations of Smith-Magenis syndrome. _h[electronic resource] |
| 260 |
_bOphthalmology _cJul 1996 |
||
| 300 |
_a1084-91 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xdiagnosis |
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 17 _xgenetics |
| 650 | 0 | 4 |
_aCorneal Diseases _xdiagnosis |
| 650 | 0 | 4 |
_aEye Diseases _xdiagnosis |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 |
_aIntellectual Disability _xdiagnosis |
| 650 | 0 | 4 |
_aIris Diseases _xdiagnosis |
| 650 | 0 | 4 | _aKaryotyping |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMyopia _xdiagnosis |
| 650 | 0 | 4 |
_aStrabismus _xdiagnosis |
| 650 | 0 | 4 | _aSyndrome |
| 700 | 1 | _aLupski, J R | |
| 700 | 1 | _aGreenberg, F | |
| 700 | 1 | _aLewis, R A | |
| 773 | 0 |
_tOphthalmology _gvol. 103 _gno. 7 _gp. 1084-91 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/s0161-6420(96)30563-0 _zAvailable from publisher's website |
| 999 |
_c8682625 _d8682625 |
||