| 000 | 01139 a2200301 4500 | ||
|---|---|---|---|
| 005 | 20250515134012.0 | ||
| 264 | 0 | _c20090310 | |
| 008 | 200903s 0 0 eng d | ||
| 022 | _a1878-0849 | ||
| 024 | 7 |
_a10.1016/j.ejmg.2008.07.008 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aKiholm Lund, Ann-Britt | |
| 245 | 0 | 0 |
_aA 15q24 microduplication, reciprocal to the recently described 15q24 microdeletion, in a boy sharing clinical features with 15q24 microdeletion syndrome patients. _h[electronic resource] |
| 260 |
_bEuropean journal of medical genetics _c |
||
| 300 |
_a520-6 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChromosome Aberrations |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 15 |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aNucleic Acid Hybridization |
| 650 | 0 | 4 | _aSyndrome |
| 700 | 1 | _aHove, Hanne Dahlgaard | |
| 700 | 1 | _aKirchhoff, Maria | |
| 773 | 0 |
_tEuropean journal of medical genetics _gvol. 51 _gno. 6 _gp. 520-6 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.ejmg.2008.07.008 _zAvailable from publisher's website |
| 999 |
_c18225971 _d18225971 |
||