| 000 | 01202 a2200361 4500 | ||
|---|---|---|---|
| 005 | 20250512084832.0 | ||
| 264 | 0 | _c19851118 | |
| 008 | 198511s 0 0 eng d | ||
| 022 | _a0148-7299 | ||
| 024 | 7 |
_a10.1002/ajmg.1320220216 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aSchmid, M | |
| 245 | 0 | 0 |
_aFamilial microtia, meatal atresia, and conductive deafness in three siblings. _h[electronic resource] |
| 260 |
_bAmerican journal of medical genetics _cOct 1985 |
||
| 300 |
_a327-32 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xgenetics |
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 |
_aEar, External _xabnormalities |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenes, Recessive |
| 650 | 0 | 4 |
_aHearing Loss _xgenetics |
| 650 | 0 | 4 |
_aHearing Loss, Conductive _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aPalate, Soft |
| 650 | 0 | 4 |
_aParalysis _xgenetics |
| 700 | 1 | _aSchröder, M | |
| 700 | 1 | _aLangenbeck, U | |
| 773 | 0 |
_tAmerican journal of medical genetics _gvol. 22 _gno. 2 _gp. 327-32 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/ajmg.1320220216 _zAvailable from publisher's website |
| 999 |
_c4056547 _d4056547 |
||