| 000 | 00971 a2200313 4500 | ||
|---|---|---|---|
| 005 | 20250517080324.0 | ||
| 264 | 0 | _c20160303 | |
| 008 | 201603s 0 0 eng d | ||
| 022 | _a1015-8146 | ||
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aGüngör, O | |
| 245 | 0 | 0 |
_aA RETT SYNDROME CASE WITH NOVEL NON-IDENTICAL MUTATION IN MECP2 GENE. _h[electronic resource] |
| 260 |
_bGenetic counseling (Geneva, Switzerland) _c2015 |
||
| 300 |
_a387-92 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aMethyl-CpG-Binding Protein 2 _xgenetics |
| 650 | 0 | 4 |
_aMutation _xgenetics |
| 650 | 0 | 4 |
_aRett Syndrome _xgenetics |
| 700 | 1 | _aKirik, S | |
| 700 | 1 | _aCevizli, D | |
| 700 | 1 | _aKaraokur, F | |
| 700 | 1 | _aOzer, L | |
| 700 | 1 | _aUysal, S | |
| 700 | 1 | _aDilber, C | |
| 773 | 0 |
_tGenetic counseling (Geneva, Switzerland) _gvol. 26 _gno. 4 _gp. 387-92 |
|
| 999 |
_c25709580 _d25709580 |
||