| 000 | 01339 a2200385 4500 | ||
|---|---|---|---|
| 005 | 20250515002013.0 | ||
| 264 | 0 | _c20051109 | |
| 008 | 200511s 0 0 eng d | ||
| 022 | _a1769-7212 | ||
| 024 | 7 |
_a10.1016/j.ejmg.2005.04.012 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aPramparo, Tiziano | |
| 245 | 0 | 0 |
_aNarrowing the deleted region associated with the 15q21 syndrome. _h[electronic resource] |
| 260 |
_bEuropean journal of medical genetics _c |
||
| 300 |
_a346-52 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xdiagnosis |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 |
_aChromosome Disorders _xdiagnosis |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 15 _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aNucleic Acid Hybridization |
| 650 | 0 | 4 | _aOligonucleotide Array Sequence Analysis |
| 650 | 0 | 4 | _aSyndrome |
| 700 | 1 | _aMattina, Teresa | |
| 700 | 1 | _aGimelli, Stefania | |
| 700 | 1 | _aLiehr, Thomas | |
| 700 | 1 | _aZuffardi, Orsetta | |
| 773 | 0 |
_tEuropean journal of medical genetics _gvol. 48 _gno. 3 _gp. 346-52 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.ejmg.2005.04.012 _zAvailable from publisher's website |
| 999 |
_c15811079 _d15811079 |
||