| 000 | 01679 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250514204804.0 | ||
| 264 | 0 | _c20050304 | |
| 008 | 200503s 0 0 eng d | ||
| 022 | _a0009-9163 | ||
| 024 | 7 |
_a10.1111/j.1399-0004.2004.00325.x _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aWattanasirichaigoon, D | |
| 245 | 0 | 0 |
_aHigh prevalence of V37I genetic variant in the connexin-26 (GJB2) gene among non-syndromic hearing-impaired and control Thai individuals. _h[electronic resource] |
| 260 |
_bClinical genetics _cNov 2004 |
||
| 300 |
_a452-60 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 |
_aAmino Acid Substitution _xgenetics |
| 650 | 0 | 4 |
_aAsian People _xgenetics |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aConnexin 26 |
| 650 | 0 | 4 |
_aConnexins _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aHearing Loss, Sensorineural _xethnology |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 |
_aIsoleucine _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMutation, Missense _xgenetics |
| 650 | 0 | 4 | _aPrevalence |
| 650 | 0 | 4 | _aThailand |
| 650 | 0 | 4 |
_aValine _xgenetics |
| 700 | 1 | _aLimwongse, C | |
| 700 | 1 | _aJariengprasert, C | |
| 700 | 1 | _aYenchitsomanus, P T | |
| 700 | 1 | _aTocharoenthanaphol, C | |
| 700 | 1 | _aThongnoppakhun, W | |
| 700 | 1 | _aThawil, C | |
| 700 | 1 | _aCharoenpipop, D | |
| 700 | 1 | _aPho-iam, T | |
| 700 | 1 | _aThongpradit, S | |
| 700 | 1 | _aDuggal, P | |
| 773 | 0 |
_tClinical genetics _gvol. 66 _gno. 5 _gp. 452-60 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/j.1399-0004.2004.00325.x _zAvailable from publisher's website |
| 999 |
_c15170198 _d15170198 |
||