| 000 | 01764 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250517150919.0 | ||
| 264 | 0 | _c20170424 | |
| 008 | 201704s 0 0 eng d | ||
| 022 | _a1932-6203 | ||
| 024 | 7 |
_a10.1371/journal.pone.0175962 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aGrau, Christina | |
| 245 | 0 | 0 |
_aXp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability. _h[electronic resource] |
| 260 |
_bPloS one _c2017 |
||
| 300 |
_ae0175962 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 |
_aAntigens, Neoplasm _xgenetics |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 |
_aChromosomal Proteins, Non-Histone _xgenetics |
| 650 | 0 | 4 |
_aChromosome Duplication _xgenetics |
| 650 | 0 | 4 |
_aChromosomes, Human, X _xgenetics |
| 650 | 0 | 4 |
_aComparative Genomic Hybridization _xmethods |
| 650 | 0 | 4 |
_aDevelopmental Disabilities _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGenes, X-Linked _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aNeoplasm Proteins _xgenetics |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 |
_aPeptide Termination Factors _xgenetics |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aSequence Deletion _xgenetics |
| 650 | 0 | 4 |
_aX Chromosome Inactivation _xgenetics |
| 700 | 1 | _aStarkovich, Molly | |
| 700 | 1 | _aAzamian, Mahshid S | |
| 700 | 1 | _aXia, Fan | |
| 700 | 1 | _aCheung, Sau Wai | |
| 700 | 1 | _aEvans, Patricia | |
| 700 | 1 | _aHenderson, Alex | |
| 700 | 1 | _aLalani, Seema R | |
| 700 | 1 | _aScott, Daryl A | |
| 773 | 0 |
_tPloS one _gvol. 12 _gno. 4 _gp. e0175962 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1371/journal.pone.0175962 _zAvailable from publisher's website |
| 999 |
_c27086221 _d27086221 |
||