| 000 | 01860 a2200589 4500 | ||
|---|---|---|---|
| 005 | 20250518000027.0 | ||
| 264 | 0 | _c20190306 | |
| 008 | 201903s 0 0 eng d | ||
| 022 | _a1559-2308 | ||
| 024 | 7 |
_a10.1080/15592294.2018.1514230 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aFontana, L | |
| 245 | 0 | 0 |
_aCharacterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders. _h[electronic resource] |
| 260 |
_bEpigenetics _c2018 |
||
| 300 |
_a897-909 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAdaptor Proteins, Signal Transducing _xchemistry |
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aApoptosis Regulatory Proteins |
| 650 | 0 | 4 |
_aBeckwith-Wiedemann Syndrome _xgenetics |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 15 _xgenetics |
| 650 | 0 | 4 | _aDNA Methylation |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenomic Imprinting |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 |
_aKruppel-Like Transcription Factors _xchemistry |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMutation, Missense |
| 650 | 0 | 4 |
_aSilver-Russell Syndrome _xgenetics |
| 650 | 0 | 4 | _aYoung Adult |
| 700 | 1 | _aBedeschi, M F | |
| 700 | 1 | _aMaitz, S | |
| 700 | 1 | _aCereda, A | |
| 700 | 1 | _aFaré, C | |
| 700 | 1 | _aMotta, S | |
| 700 | 1 | _aSeresini, A | |
| 700 | 1 | _aD'Ursi, P | |
| 700 | 1 | _aOrro, A | |
| 700 | 1 | _aPecile, V | |
| 700 | 1 | _aCalvello, M | |
| 700 | 1 | _aSelicorni, A | |
| 700 | 1 | _aLalatta, F | |
| 700 | 1 | _aMilani, D | |
| 700 | 1 | _aSirchia, S M | |
| 700 | 1 | _aMiozzo, M | |
| 700 | 1 | _aTabano, S | |
| 773 | 0 |
_tEpigenetics _gvol. 13 _gno. 9 _gp. 897-909 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1080/15592294.2018.1514230 _zAvailable from publisher's website |
| 999 |
_c28841656 _d28841656 |
||