| 000 | 01683 a2200505 4500 | ||
|---|---|---|---|
| 005 | 20250516212040.0 | ||
| 264 | 0 | _c20150611 | |
| 008 | 201506s 0 0 eng d | ||
| 022 | _a1476-5438 | ||
| 024 | 7 |
_a10.1038/ejhg.2014.63 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aSchroeder, Christopher | |
| 245 | 0 | 0 |
_aGenome-wide UPD screening in patients with intellectual disability. _h[electronic resource] |
| 260 |
_bEuropean journal of human genetics : EJHG _cOct 2014 |
||
| 300 |
_a1233-5 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 7 _xgenetics |
| 650 | 0 | 4 | _aDNA Copy Number Variations |
| 650 | 0 | 4 | _aGenetic Testing |
| 650 | 0 | 4 | _aGenome, Human |
| 650 | 0 | 4 | _aGenome-Wide Association Study |
| 650 | 0 | 4 | _aGenomic Imprinting |
| 650 | 0 | 4 | _aHomozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
| 650 | 0 | 4 | _aParents |
| 650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
| 650 | 0 | 4 | _aRetrospective Studies |
| 650 | 0 | 4 |
_aUniparental Disomy _xgenetics |
| 700 | 1 | _aEkici, Arif Bülent | |
| 700 | 1 | _aMoog, Ute | |
| 700 | 1 | _aGrasshoff, Ute | |
| 700 | 1 | _aMau-Holzmann, Ulrike | |
| 700 | 1 | _aSturm, Marc | |
| 700 | 1 | _aVosseler, Vanessa | |
| 700 | 1 | _aPoths, Sven | |
| 700 | 1 | _aRappold, Gudrun | |
| 700 | 1 | _aRiess, Angelika | |
| 700 | 1 | _aRiess, Olaf | |
| 700 | 1 | _aDufke, Andreas | |
| 700 | 1 | _aBonin, Michael | |
| 773 | 0 |
_tEuropean journal of human genetics : EJHG _gvol. 22 _gno. 10 _gp. 1233-5 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1038/ejhg.2014.63 _zAvailable from publisher's website |
| 999 |
_c23801080 _d23801080 |
||