| 000 | 01792 a2200529 4500 | ||
|---|---|---|---|
| 005 | 20250517092421.0 | ||
| 264 | 0 | _c20170621 | |
| 008 | 201706s 0 0 eng d | ||
| 022 | _a1432-1203 | ||
| 024 | 7 |
_a10.1007/s00439-016-1668-4 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aLabonne, Jonathan D J | |
| 245 | 0 | 0 |
_aAn atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disability. _h[electronic resource] |
| 260 |
_bHuman genetics _c07 2016 |
||
| 300 |
_a757-71 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aAged |
| 650 | 0 | 4 | _aAnimals |
| 650 | 0 | 4 |
_aAutistic Disorder _xgenetics |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 12 _xgenetics |
| 650 | 0 | 4 | _aComparative Genomic Hybridization |
| 650 | 0 | 4 | _aDisease Models, Animal |
| 650 | 0 | 4 |
_aEpilepsy _xgenetics |
| 650 | 0 | 4 |
_aF-Box Proteins _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aFetus |
| 650 | 0 | 4 |
_aHistone-Lysine N-Methyltransferase _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aIn Situ Hybridization, Fluorescence |
| 650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
| 650 | 0 | 4 |
_aJumonji Domain-Containing Histone Demethylases _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 | _aZebrafish |
| 700 | 1 | _aLee, Kang-Han | |
| 700 | 1 | _aIwase, Shigeki | |
| 700 | 1 | _aKong, Il-Keun | |
| 700 | 1 | _aDiamond, Michael P | |
| 700 | 1 | _aLayman, Lawrence C | |
| 700 | 1 | _aKim, Cheol-Hee | |
| 700 | 1 | _aKim, Hyung-Goo | |
| 773 | 0 |
_tHuman genetics _gvol. 135 _gno. 7 _gp. 757-71 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s00439-016-1668-4 _zAvailable from publisher's website |
| 999 |
_c25951684 _d25951684 |
||