| 000 | 01807 a2200493 4500 | ||
|---|---|---|---|
| 005 | 20250517102851.0 | ||
| 264 | 0 | _c20171016 | |
| 008 | 201710s 0 0 eng d | ||
| 022 | _a1542-0760 | ||
| 024 | 7 |
_a10.1002/bdra.23535 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aGoumy, Carole | |
| 245 | 0 | 0 |
_aA novel 2q14.1q14.3 deletion involving GLI2 and RNU4ATAC genes associated with partial corpus callosum agenesis and severe intrauterine growth retardation. _h[electronic resource] |
| 260 |
_bBirth defects research. Part A, Clinical and molecular teratology _cSep 2016 |
||
| 300 |
_a793-7 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 |
_aAgenesis of Corpus Callosum _xgenetics |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 2 _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aFetal Growth Retardation _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aKruppel-Like Transcription Factors _xgenetics |
| 650 | 0 | 4 |
_aNuclear Proteins _xgenetics |
| 650 | 0 | 4 | _aPregnancy |
| 650 | 0 | 4 |
_aRNA, Small Nuclear _xgenetics |
| 650 | 0 | 4 | _aZinc Finger Protein Gli2 |
| 700 | 1 | _aGay-Bellile, Mathilde | |
| 700 | 1 | _aSalaun, Gaelle | |
| 700 | 1 | _aKemeny, Stephan | |
| 700 | 1 | _aEymard-Pierre, Eleonore | |
| 700 | 1 | _aBiard, Marie | |
| 700 | 1 | _aPebrel-Richard, Celine | |
| 700 | 1 | _aVanlieferinghen, Philippe | |
| 700 | 1 | _aFrancannet, Christine | |
| 700 | 1 | _aTchirkov, Andrei | |
| 700 | 1 | _aLaurichesse, Helene | |
| 700 | 1 | _aRouzade, Charles | |
| 700 | 1 | _aGouas, Laetitia | |
| 700 | 1 | _aVago, Philippe | |
| 773 | 0 |
_tBirth defects research. Part A, Clinical and molecular teratology _gvol. 106 _gno. 9 _gp. 793-7 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/bdra.23535 _zAvailable from publisher's website |
| 999 |
_c26163575 _d26163575 |
||