| 000 | 02946 a2201069 4500 | ||
|---|---|---|---|
| 005 | 20250515165419.0 | ||
| 264 | 0 | _c20091102 | |
| 008 | 200911s 0 0 eng d | ||
| 022 | _a1468-6244 | ||
| 024 | 7 |
_a10.1136/jmg.2008.063412 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _avan Bon, B W M | |
| 245 | 0 | 0 |
_aFurther delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome. _h[electronic resource] |
| 260 |
_bJournal of medical genetics _cAug 2009 |
||
| 300 |
_a511-23 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChromosome Aberrations |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 |
_aChromosome Disorders _xgenetics |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 15 _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGene Duplication |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aOligonucleotide Array Sequence Analysis |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPregnancy |
| 650 | 0 | 4 | _aSyndrome |
| 700 | 1 | _aMefford, H C | |
| 700 | 1 | _aMenten, B | |
| 700 | 1 | _aKoolen, D A | |
| 700 | 1 | _aSharp, A J | |
| 700 | 1 | _aNillesen, W M | |
| 700 | 1 | _aInnis, J W | |
| 700 | 1 | _ade Ravel, T J L | |
| 700 | 1 | _aMercer, C L | |
| 700 | 1 | _aFichera, M | |
| 700 | 1 | _aStewart, H | |
| 700 | 1 | _aConnell, L E | |
| 700 | 1 | _aOunap, K | |
| 700 | 1 | _aLachlan, K | |
| 700 | 1 | _aCastle, B | |
| 700 | 1 | _aVan der Aa, N | |
| 700 | 1 | _avan Ravenswaaij, C | |
| 700 | 1 | _aNobrega, M A | |
| 700 | 1 | _aSerra-Juhé, C | |
| 700 | 1 | _aSimonic, I | |
| 700 | 1 | _ade Leeuw, N | |
| 700 | 1 | _aPfundt, R | |
| 700 | 1 | _aBongers, E M | |
| 700 | 1 | _aBaker, C | |
| 700 | 1 | _aFinnemore, P | |
| 700 | 1 | _aHuang, S | |
| 700 | 1 | _aMaloney, V K | |
| 700 | 1 | _aCrolla, J A | |
| 700 | 1 | _avan Kalmthout, M | |
| 700 | 1 | _aElia, M | |
| 700 | 1 | _aVandeweyer, G | |
| 700 | 1 | _aFryns, J P | |
| 700 | 1 | _aJanssens, S | |
| 700 | 1 | _aFoulds, N | |
| 700 | 1 | _aReitano, S | |
| 700 | 1 | _aSmith, K | |
| 700 | 1 | _aParkel, S | |
| 700 | 1 | _aLoeys, B | |
| 700 | 1 | _aWoods, C G | |
| 700 | 1 | _aOostra, A | |
| 700 | 1 | _aSpeleman, F | |
| 700 | 1 | _aPereira, A C | |
| 700 | 1 | _aKurg, A | |
| 700 | 1 | _aWillatt, L | |
| 700 | 1 | _aKnight, S J L | |
| 700 | 1 | _aVermeesch, J R | |
| 700 | 1 | _aRomano, C | |
| 700 | 1 | _aBarber, J C | |
| 700 | 1 | _aMortier, G | |
| 700 | 1 | _aPérez-Jurado, L A | |
| 700 | 1 | _aKooy, F | |
| 700 | 1 | _aBrunner, H G | |
| 700 | 1 | _aEichler, E E | |
| 700 | 1 | _aKleefstra, T | |
| 700 | 1 | _ade Vries, B B A | |
| 773 | 0 |
_tJournal of medical genetics _gvol. 46 _gno. 8 _gp. 511-23 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1136/jmg.2008.063412 _zAvailable from publisher's website |
| 999 |
_c18803887 _d18803887 |
||