000 | 01247 a2200325 4500 | ||
---|---|---|---|
005 | 20250517055150.0 | ||
264 | 0 | _c20161019 | |
008 | 201610s 0 0 eng d | ||
022 | _a1552-4833 | ||
024 | 7 |
_a10.1002/ajmg.a.37416 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aMüller, Anne | |
245 | 0 | 0 |
_aNo major contribution of IGF2 variants to the etiology of sporadic 11p15-associated imprinting disorders. _h[electronic resource] |
260 |
_bAmerican journal of medical genetics. Part A _cJan 2016 |
||
300 |
_a283-4 p. _bdigital |
||
500 | _aPublication Type: Letter; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 |
_aBeckwith-Wiedemann Syndrome _xgenetics |
650 | 0 | 4 |
_aChromosomes, Human, Pair 11 _xgenetics |
650 | 0 | 4 |
_aFetal Growth Retardation _xgenetics |
650 | 0 | 4 | _aGenetic Testing |
650 | 0 | 4 |
_aGenomic Imprinting _xgenetics |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 |
_aInsulin-Like Growth Factor II _xgenetics |
700 | 1 | _aSoellner, Lukas | |
700 | 1 | _aBinder, Gerhard | |
700 | 1 | _aBegemann, Matthias | |
700 | 1 | _aEggermann, Thomas | |
773 | 0 |
_tAmerican journal of medical genetics. Part A _gvol. 170A _gno. 1 _gp. 283-4 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1002/ajmg.a.37416 _zAvailable from publisher's website |
999 |
_c25334843 _d25334843 |