| 000 | 01631 a2200493 4500 | ||
|---|---|---|---|
| 005 | 20250516113545.0 | ||
| 264 | 0 | _c20130621 | |
| 008 | 201306s 0 0 eng d | ||
| 022 | _a1552-4833 | ||
| 024 | 7 |
_a10.1002/ajmg.a.35362 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aNimmakayalu, Manjunath | |
| 245 | 0 | 0 |
_a2q24 deletions: further characterization of clinical findings and their relation to the SCN cluster. _h[electronic resource] |
| 260 |
_bAmerican journal of medical genetics. Part A _cNov 2012 |
||
| 300 |
_a2767-74 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xdiagnosis |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 2 |
| 650 | 0 | 4 | _aComparative Genomic Hybridization |
| 650 | 0 | 4 | _aFacies |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Association Studies |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aIn Situ Hybridization, Fluorescence |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMultigene Family |
| 650 | 0 | 4 |
_aSodium Channels _xgenetics |
| 700 | 1 | _aNoble, Nathan | |
| 700 | 1 | _aHorton, V Kim | |
| 700 | 1 | _aWilling, Marcia | |
| 700 | 1 | _aCopeland, Sara | |
| 700 | 1 | _aSheffield, Val | |
| 700 | 1 | _aNagy, Peter L | |
| 700 | 1 | _aWassink, Tom | |
| 700 | 1 | _aPatil, Shivanand | |
| 700 | 1 | _aShchelochkov, Oleg A | |
| 773 | 0 |
_tAmerican journal of medical genetics. Part A _gvol. 158A _gno. 11 _gp. 2767-74 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/ajmg.a.35362 _zAvailable from publisher's website |
| 999 |
_c22146641 _d22146641 |
||