| 000 | 01523 a2200481 4500 | ||
|---|---|---|---|
| 005 | 20250516101744.0 | ||
| 264 | 0 | _c20140114 | |
| 008 | 201401s 0 0 eng d | ||
| 022 | _a1399-0004 | ||
| 024 | 7 |
_a10.1111/j.1399-0004.2012.01925.x _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aHoppman-Chaney, N | |
| 245 | 0 | 0 |
_aIdentification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype. _h[electronic resource] |
| 260 |
_bClinical genetics _cApr 2013 |
||
| 300 |
_a345-51 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 15 |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGene Deletion |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 | _aHomozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aSyndrome |
| 650 | 0 | 4 | _aYoung Adult |
| 650 | 0 | 4 |
_aalpha7 Nicotinic Acetylcholine Receptor _xgenetics |
| 700 | 1 | _aWain, K | |
| 700 | 1 | _aSeger, P R | |
| 700 | 1 | _aSuperneau, D W | |
| 700 | 1 | _aHodge, J C | |
| 773 | 0 |
_tClinical genetics _gvol. 83 _gno. 4 _gp. 345-51 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/j.1399-0004.2012.01925.x _zAvailable from publisher's website |
| 999 |
_c21928469 _d21928469 |
||