| 000 | 01192 a2200337 4500 | ||
|---|---|---|---|
| 005 | 20250517045426.0 | ||
| 264 | 0 | _c20160620 | |
| 008 | 201606s 0 0 eng d | ||
| 022 | _a1473-5717 | ||
| 024 | 7 |
_a10.1097/MCD.0000000000000096 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aAkilapa, Rhoda S | |
| 245 | 0 | 0 |
_aClinical report: inherited deletion of chromosome 12q21.31q21.32 associated with a distinct phenotype and intellectual disability. _h[electronic resource] |
| 260 |
_bClinical dysmorphology _cOct 2015 |
||
| 300 |
_a151-5 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 12 |
| 650 | 0 | 4 | _aDNA Copy Number Variations |
| 650 | 0 | 4 | _aGenetic Association Studies |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aSequence Deletion |
| 700 | 1 | _aSmith, Kath | |
| 700 | 1 | _aBalasubramanian, Meena | |
| 773 | 0 |
_tClinical dysmorphology _gvol. 24 _gno. 4 _gp. 151-5 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1097/MCD.0000000000000096 _zAvailable from publisher's website |
| 999 |
_c25164007 _d25164007 |
||