| 000 | 01563 a2200445 4500 | ||
|---|---|---|---|
| 005 | 20250514060057.0 | ||
| 264 | 0 | _c20030807 | |
| 008 | 200308s 0 0 eng d | ||
| 022 | _a1552-4825 | ||
| 024 | 7 |
_a10.1002/ajmg.a.10155 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aPetek, Erwin | |
| 245 | 0 | 0 |
_aMolecular characterization of a 12q22-q24 deletion associated with congenital deafness: confirmation and refinement of the DFNA25 locus. _h[electronic resource] |
| 260 |
_bAmerican journal of medical genetics. Part A _cMar 2003 |
||
| 300 |
_a122-6 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChromosome Banding |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 |
_aChromosome Mapping _xmethods |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 12 _xgenetics |
| 650 | 0 | 4 | _aFamily Health |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGenes, Dominant _xgenetics |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 |
_aHearing Loss _xcongenital |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aIn Situ Hybridization, Fluorescence |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMicrosatellite Repeats |
| 650 | 0 | 4 | _aPedigree |
| 700 | 1 | _aWindpassinger, Christian | |
| 700 | 1 | _aMach, Monika | |
| 700 | 1 | _aRauter, Ludwig | |
| 700 | 1 | _aScherer, Stephen W | |
| 700 | 1 | _aWagner, Klaus | |
| 700 | 1 | _aKroisel, Peter M | |
| 773 | 0 |
_tAmerican journal of medical genetics. Part A _gvol. 117A _gno. 2 _gp. 122-6 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/ajmg.a.10155 _zAvailable from publisher's website |
| 999 |
_c12365670 _d12365670 |
||