| 000 | 01527 a2200433 4500 | ||
|---|---|---|---|
| 005 | 20250517070324.0 | ||
| 264 | 0 | _c20160922 | |
| 008 | 201609s 0 0 spa d | ||
| 022 | _a1576-6578 | ||
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aNatera-De Benito, Daniel | |
| 245 | 0 | 0 |
_a[Phenotypic variability of the 1q21.1 microdeletion syndrome in members of the same family: relevance of detection of neuropsychiatric disorders for diagnosis of genetic syndromes]. _h[electronic resource] |
| 260 |
_bRevista de neurologia _cDec 2015 |
||
| 300 |
_a550-6 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; English Abstract; Journal Article | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 1 _xgenetics |
| 650 | 0 | 4 | _aComparative Genomic Hybridization |
| 650 | 0 | 4 |
_aDisruptive, Impulse Control, and Conduct Disorders _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aHypertelorism _xgenetics |
| 650 | 0 | 4 | _aIn Situ Hybridization, Fluorescence |
| 650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPenetrance |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aSyndrome |
| 700 | 1 | _aVidal-Esteban, Arantxa | |
| 700 | 1 | _aSanchez-Del Pozo, Jaime | |
| 700 | 1 | _aMoreno-Garcia, Marta | |
| 700 | 1 | _aSuela-Rubio, Javier | |
| 700 | 1 | _aCruz-Rojo, Jaime | |
| 700 | 1 | _aRivero-Martin, María José | |
| 773 | 0 |
_tRevista de neurologia _gvol. 61 _gno. 12 _gp. 550-6 |
|
| 999 |
_c25537224 _d25537224 |
||