| 000 | 01784 a2200541 4500 | ||
|---|---|---|---|
| 005 | 20250514223022.0 | ||
| 264 | 0 | _c20060803 | |
| 008 | 200608s 0 0 eng d | ||
| 022 | _a1468-6244 | ||
| 024 | 7 |
_a10.1136/jmg.2004.028464 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aKleefstra, T | |
| 245 | 0 | 0 |
_aDisruption of the gene Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) is associated with the 9q34 subtelomeric deletion syndrome. _h[electronic resource] |
| 260 |
_bJournal of medical genetics _cApr 2005 |
||
| 300 |
_a299-306 p. _bdigital |
||
| 500 | _aPublication Type: Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xgenetics |
| 650 | 0 | 4 | _aAnimals |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 9 _xgenetics |
| 650 | 0 | 4 | _aExpressed Sequence Tags |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHistone-Lysine N-Methyltransferase |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
| 650 | 0 | 4 |
_aMethyltransferases _xgenetics |
| 650 | 0 | 4 | _aMice |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aSyndrome |
| 650 | 0 | 4 |
_aTelomere _xgenetics |
| 650 | 0 | 4 | _aTranslocation, Genetic |
| 700 | 1 | _aSmidt, M | |
| 700 | 1 | _aBanning, M J G | |
| 700 | 1 | _aOudakker, A R | |
| 700 | 1 | _aVan Esch, H | |
| 700 | 1 | _ade Brouwer, A P M | |
| 700 | 1 | _aNillesen, W | |
| 700 | 1 | _aSistermans, E A | |
| 700 | 1 | _aHamel, B C J | |
| 700 | 1 | _ade Bruijn, D | |
| 700 | 1 | _aFryns, J-P | |
| 700 | 1 | _aYntema, H G | |
| 700 | 1 | _aBrunner, H G | |
| 700 | 1 | _ade Vries, B B A | |
| 700 | 1 | _avan Bokhoven, H | |
| 773 | 0 |
_tJournal of medical genetics _gvol. 42 _gno. 4 _gp. 299-306 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1136/jmg.2004.028464 _zAvailable from publisher's website |
| 999 |
_c15475327 _d15475327 |
||