| 000 | 01678 a2200529 4500 | ||
|---|---|---|---|
| 005 | 20250516181832.0 | ||
| 264 | 0 | _c20150413 | |
| 008 | 201504s 0 0 eng d | ||
| 022 | _a1552-4833 | ||
| 024 | 7 |
_a10.1002/ajmg.a.36201 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aChowdhury, Shimul | |
| 245 | 0 | 0 |
_aPhenotypic and molecular characterization of 19q12q13.1 deletions: a report of five patients. _h[electronic resource] |
| 260 |
_bAmerican journal of medical genetics. Part A _cJan 2014 |
||
| 300 |
_a62-9 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xgenetics |
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 19 |
| 650 | 0 | 4 | _aComparative Genomic Hybridization |
| 650 | 0 | 4 | _aFacies |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aGenetic Diseases, Inborn _xdiagnosis |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aSyndrome |
| 700 | 1 | _aBandholz, Anne M | |
| 700 | 1 | _aParkash, Sandhya | |
| 700 | 1 | _aDyack, Sarah | |
| 700 | 1 | _aRideout, Andrea L | |
| 700 | 1 | _aLeppig, Kathleen A | |
| 700 | 1 | _aThiese, Heidi | |
| 700 | 1 | _aWheeler, Patricia G | |
| 700 | 1 | _aTsang, Marilyn | |
| 700 | 1 | _aBallif, Blake C | |
| 700 | 1 | _aShaffer, Lisa G | |
| 700 | 1 | _aTorchia, Beth S | |
| 700 | 1 | _aEllison, Jay W | |
| 700 | 1 | _aRosenfeld, Jill A | |
| 773 | 0 |
_tAmerican journal of medical genetics. Part A _gvol. 164A _gno. 1 _gp. 62-9 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/ajmg.a.36201 _zAvailable from publisher's website |
| 999 |
_c23277036 _d23277036 |
||