| 000 | 01911 a2200553 4500 | ||
|---|---|---|---|
| 005 | 20250515041442.0 | ||
| 264 | 0 | _c20061114 | |
| 008 | 200611s 0 0 eng d | ||
| 022 | _a1442-6404 | ||
| 024 | 7 |
_a10.1111/j.1442-9071.2006.01314.x _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aDickinson, Joanne L | |
| 245 | 0 | 0 |
_aMutations in the NDP gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity. _h[electronic resource] |
| 260 |
_bClinical & experimental ophthalmology _c |
||
| 300 |
_a682-8 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_a5' Untranslated Regions _xgenetics |
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChromatography, High Pressure Liquid |
| 650 | 0 | 4 |
_aDeafness _xgenetics |
| 650 | 0 | 4 |
_aEye Proteins _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGestational Age |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 | _aMutation, Missense |
| 650 | 0 | 4 |
_aNerve Tissue Proteins _xgenetics |
| 650 | 0 | 4 |
_aRetinal Diseases _xgenetics |
| 650 | 0 | 4 |
_aRetinopathy of Prematurity _xgenetics |
| 650 | 0 | 4 | _aSequence Analysis, DNA |
| 650 | 0 | 4 |
_aVitreoretinopathy, Proliferative _xgenetics |
| 700 | 1 | _aSale, Michèle M | |
| 700 | 1 | _aPassmore, Abraham | |
| 700 | 1 | _aFitzGerald, Liesel M | |
| 700 | 1 | _aWheatley, Catherine M | |
| 700 | 1 | _aBurdon, Kathryn P | |
| 700 | 1 | _aCraig, Jamie E | |
| 700 | 1 | _aTengtrisorn, Supaporn | |
| 700 | 1 | _aCarden, Susan M | |
| 700 | 1 | _aMaclean, Hector | |
| 700 | 1 | _aMackey, David A | |
| 773 | 0 |
_tClinical & experimental ophthalmology _gvol. 34 _gno. 7 _gp. 682-8 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/j.1442-9071.2006.01314.x _zAvailable from publisher's website |
| 999 |
_c16553190 _d16553190 |
||