| 000 | 01362 a2200409 4500 | ||
|---|---|---|---|
| 005 | 20250513081603.0 | ||
| 264 | 0 | _c19930520 | |
| 008 | 199305s 0 0 eng d | ||
| 022 | _a0022-2593 | ||
| 024 | 7 |
_a10.1136/jmg.30.3.253 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aBonneau, D | |
| 245 | 0 | 0 |
_aUsher syndrome type I associated with bronchiectasis and immotile nasal cilia in two brothers. _h[electronic resource] |
| 260 |
_bJournal of medical genetics _cMar 1993 |
||
| 300 |
_a253-4 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xgenetics |
| 650 | 0 | 4 |
_aBronchiectasis _xdiagnostic imaging |
| 650 | 0 | 4 |
_aCilia _xultrastructure |
| 650 | 0 | 4 |
_aCiliary Motility Disorders _xgenetics |
| 650 | 0 | 4 |
_aDeafness _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aNasal Mucosa _xultrastructure |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aRadiography |
| 650 | 0 | 4 |
_aRetinitis Pigmentosa _xgenetics |
| 650 | 0 | 4 | _aSyndrome |
| 650 | 0 | 4 |
_aVestibule, Labyrinth _xabnormalities |
| 700 | 1 | _aRaymond, F | |
| 700 | 1 | _aKremer, C | |
| 700 | 1 | _aKlossek, J M | |
| 700 | 1 | _aKaplan, J | |
| 700 | 1 | _aPatte, F | |
| 773 | 0 |
_tJournal of medical genetics _gvol. 30 _gno. 3 _gp. 253-4 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1136/jmg.30.3.253 _zAvailable from publisher's website |
| 999 |
_c8473380 _d8473380 |
||