| 000 | 01760 a2200541 4500 | ||
|---|---|---|---|
| 005 | 20250515102728.0 | ||
| 264 | 0 | _c20080312 | |
| 008 | 200803s 0 0 eng d | ||
| 022 | _a1460-2083 | ||
| 024 | 7 |
_a10.1093/hmg/ddm376 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aKumar, Ravinesh A | |
| 245 | 0 | 0 |
_aRecurrent 16p11.2 microdeletions in autism. _h[electronic resource] |
| 260 |
_bHuman molecular genetics _cFeb 2008 |
||
| 300 |
_a628-38 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAutistic Disorder _xgenetics |
| 650 | 0 | 4 | _aBase Sequence |
| 650 | 0 | 4 | _aCase-Control Studies |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChromosome Breakage |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 |
_aChromosomes, Artificial, Bacterial _xgenetics |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 16 _xgenetics |
| 650 | 0 | 4 |
_aDNA Primers _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGene Frequency |
| 650 | 0 | 4 | _aGenetic Predisposition to Disease |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aIn Situ Hybridization, Fluorescence |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMicrosatellite Repeats |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPolymerase Chain Reaction |
| 700 | 1 | _aKaraMohamed, Samer | |
| 700 | 1 | _aSudi, Jyotsna | |
| 700 | 1 | _aConrad, Donald F | |
| 700 | 1 | _aBrune, Camille | |
| 700 | 1 | _aBadner, Judith A | |
| 700 | 1 | _aGilliam, T Conrad | |
| 700 | 1 | _aNowak, Norma J | |
| 700 | 1 | _aCook, Edwin H | |
| 700 | 1 | _aDobyns, William B | |
| 700 | 1 | _aChristian, Susan L | |
| 773 | 0 |
_tHuman molecular genetics _gvol. 17 _gno. 4 _gp. 628-38 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1093/hmg/ddm376 _zAvailable from publisher's website |
| 999 |
_c17667672 _d17667672 |
||