| 000 | 01583 a2200457 4500 | ||
|---|---|---|---|
| 005 | 20250515031150.0 | ||
| 264 | 0 | _c20060928 | |
| 008 | 200609s 0 0 eng d | ||
| 022 | _a1552-4825 | ||
| 024 | 7 |
_a10.1002/ajmg.a.31314 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aDonzel-Javouhey, Anne | |
| 245 | 0 | 0 |
_aA new cohort of MECP2 mutation screening in unexplained mental retardation: careful re-evaluation is the best indicator for molecular diagnosis. _h[electronic resource] |
| 260 |
_bAmerican journal of medical genetics. Part A _cJul 2006 |
||
| 300 |
_a1603-7 p. _bdigital |
||
| 500 | _aPublication Type: Letter; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aBase Sequence |
| 650 | 0 | 4 | _aCohort Studies |
| 650 | 0 | 4 |
_aDNA _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Testing |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMethyl-CpG-Binding Protein 2 _xgenetics |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aRett Syndrome _xgenetics |
| 700 | 1 | _aThauvin-Robinet, Christel | |
| 700 | 1 | _aCusin, Veronica | |
| 700 | 1 | _aMadinier, Nathalie | |
| 700 | 1 | _aManceau, Eric | |
| 700 | 1 | _aDipanda, Dominique | |
| 700 | 1 | _aDulieu, Véronique | |
| 700 | 1 | _aMugneret, Francine | |
| 700 | 1 | _aHuet, Frédéric | |
| 700 | 1 | _aTeyssier, Jean-Raymond | |
| 700 | 1 | _aFaivre, Laurence | |
| 773 | 0 |
_tAmerican journal of medical genetics. Part A _gvol. 140 _gno. 14 _gp. 1603-7 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/ajmg.a.31314 _zAvailable from publisher's website |
| 999 |
_c16359618 _d16359618 |
||