| 000 | 01829 a2200541 4500 | ||
|---|---|---|---|
| 005 | 20250514063154.0 | ||
| 264 | 0 | _c20031029 | |
| 008 | 200310s 0 0 ger d | ||
| 022 | _a1432-9417 | ||
| 024 | 7 |
_a10.1007/s10006-002-0444-x _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aPetschler, M | |
| 245 | 0 | 0 |
_a[Clinical and molecular genetic observations on families with cherubism over three generations]. _h[electronic resource] |
| 260 |
_bMund-, Kiefer- und Gesichtschirurgie : MKG _cMar 2003 |
||
| 300 |
_a83-7 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; English Abstract; Journal Article | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 |
_aCherubism _xdiagnosis |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChromosome Aberrations |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 4 |
| 650 | 0 | 4 | _aCombined Modality Therapy |
| 650 | 0 | 4 |
_aCraniosynostoses _xdiagnosis |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aFollow-Up Studies |
| 650 | 0 | 4 | _aGenes, Dominant |
| 650 | 0 | 4 |
_aGenetic Predisposition to Disease _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aOrthodontics, Corrective |
| 650 | 0 | 4 |
_aOsteoarthropathy, Secondary Hypertrophic _xdiagnosis |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aProtein-Tyrosine Kinases |
| 650 | 0 | 4 | _aReceptor, Fibroblast Growth Factor, Type 3 |
| 650 | 0 | 4 |
_aReceptors, Fibroblast Growth Factor _xgenetics |
| 650 | 0 | 4 |
_aTooth Abnormalities _xdiagnosis |
| 700 | 1 | _aStiller, M | |
| 700 | 1 | _aHoffmeister, B | |
| 700 | 1 | _aWitkowski, R | |
| 700 | 1 | _aOpitz, C | |
| 700 | 1 | _aBill, J S | |
| 700 | 1 | _aPeters, H | |
| 773 | 0 |
_tMund-, Kiefer- und Gesichtschirurgie : MKG _gvol. 7 _gno. 2 _gp. 83-7 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s10006-002-0444-x _zAvailable from publisher's website |
| 999 |
_c12457625 _d12457625 |
||