| 000 | 01560 a2200457 4500 | ||
|---|---|---|---|
| 005 | 20250516060200.0 | ||
| 264 | 0 | _c20120210 | |
| 008 | 201202s 0 0 eng d | ||
| 022 | _a1468-6244 | ||
| 024 | 7 |
_a10.1136/jmedgenet-2011-100147 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aHehir-Kwa, Jayne Y | |
| 245 | 0 | 0 |
_aDe novo copy number variants associated with intellectual disability have a paternal origin and age bias. _h[electronic resource] |
| 260 |
_bJournal of medical genetics _cNov 2011 |
||
| 300 |
_a776-8 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aAlleles |
| 650 | 0 | 4 | _aCohort Studies |
| 650 | 0 | 4 | _aDNA Copy Number Variations |
| 650 | 0 | 4 | _aGene Dosage |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aIntellectual Disability _xepidemiology |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aNetherlands |
| 650 | 0 | 4 | _aOligonucleotide Array Sequence Analysis |
| 650 | 0 | 4 | _aPaternal Age |
| 650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
| 650 | 0 | 4 | _aSegmental Duplications, Genomic |
| 650 | 0 | 4 | _aSex Factors |
| 650 | 0 | 4 | _aSpermatogenesis |
| 700 | 1 | _aRodríguez-Santiago, Benjamín | |
| 700 | 1 | _aVissers, Lisenka E | |
| 700 | 1 | _ade Leeuw, Nicole | |
| 700 | 1 | _aPfundt, Rolph | |
| 700 | 1 | _aBuitelaar, Jan K | |
| 700 | 1 | _aPérez-Jurado, Luis A | |
| 700 | 1 | _aVeltman, Joris A | |
| 773 | 0 |
_tJournal of medical genetics _gvol. 48 _gno. 11 _gp. 776-8 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1136/jmedgenet-2011-100147 _zAvailable from publisher's website |
| 999 |
_c21205518 _d21205518 |
||