000 | 01952 a2200637 4500 | ||
---|---|---|---|
005 | 20250517021733.0 | ||
264 | 0 | _c20150916 | |
008 | 201509s 0 0 eng d | ||
022 | _a1552-4833 | ||
024 | 7 |
_a10.1002/ajmg.a.36866 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aRosenfeld, Jill A | |
245 | 0 | 0 |
_aClinical features associated with copy number variations of the 14q32 imprinted gene cluster. _h[electronic resource] |
260 |
_bAmerican journal of medical genetics. Part A _cFeb 2015 |
||
300 |
_a345-53 p. _bdigital |
||
500 | _aPublication Type: Journal Article | ||
650 | 0 | 4 | _aAdolescent |
650 | 0 | 4 | _aAdult |
650 | 0 | 4 | _aChild |
650 | 0 | 4 | _aChild, Preschool |
650 | 0 | 4 | _aChromosome Deletion |
650 | 0 | 4 |
_aChromosome Disorders _xdiagnosis |
650 | 0 | 4 | _aChromosome Duplication |
650 | 0 | 4 | _aChromosomes, Human, Pair 14 |
650 | 0 | 4 | _aComparative Genomic Hybridization |
650 | 0 | 4 | _aDNA Copy Number Variations |
650 | 0 | 4 | _aFacies |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aGenetic Association Studies |
650 | 0 | 4 | _aGenetic Loci |
650 | 0 | 4 | _aGenomic Imprinting |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aInfant |
650 | 0 | 4 | _aInfant, Newborn |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMiddle Aged |
650 | 0 | 4 | _aMultigene Family |
650 | 0 | 4 | _aPhenotype |
650 | 0 | 4 | _aUniparental Disomy |
650 | 0 | 4 | _aYoung Adult |
700 | 1 | _aFox, Joyce E | |
700 | 1 | _aDescartes, Maria | |
700 | 1 | _aBrewer, Fallon | |
700 | 1 | _aStroud, Tracy | |
700 | 1 | _aGorski, Jerome L | |
700 | 1 | _aUpton, Sheila J | |
700 | 1 | _aMoeschler, John B | |
700 | 1 | _aMonteleone, Berrin | |
700 | 1 | _aNeill, Nicholas J | |
700 | 1 | _aLamb, Allen N | |
700 | 1 | _aBallif, Blake C | |
700 | 1 | _aShaffer, Lisa G | |
700 | 1 | _aRavnan, J Britt | |
773 | 0 |
_tAmerican journal of medical genetics. Part A _gvol. 167A _gno. 2 _gp. 345-53 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1002/ajmg.a.36866 _zAvailable from publisher's website |
999 |
_c24693536 _d24693536 |