| 000 | 01752 a2200529 4500 | ||
|---|---|---|---|
| 005 | 20250514231049.0 | ||
| 264 | 0 | _c20050810 | |
| 008 | 200508s 0 0 eng d | ||
| 022 | _a1552-4825 | ||
| 024 | 7 |
_a10.1002/ajmg.a.30774 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aArcher, H L | |
| 245 | 0 | 0 |
_aDistinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pter. _h[electronic resource] |
| 260 |
_bAmerican journal of medical genetics. Part A _cJul 2005 |
||
| 300 |
_a38-44 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Review | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xgenetics |
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 19 _xgenetics |
| 650 | 0 | 4 |
_aCleft Palate _xpathology |
| 650 | 0 | 4 |
_aFace _xabnormalities |
| 650 | 0 | 4 |
_aGenetic Predisposition to Disease _xgenetics |
| 650 | 0 | 4 |
_aHearing Loss _xpathology |
| 650 | 0 | 4 |
_aHeart Defects, Congenital _xpathology |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aImmune System _xabnormalities |
| 650 | 0 | 4 | _aIn Situ Hybridization, Fluorescence |
| 650 | 0 | 4 |
_aKeloid _xpathology |
| 650 | 0 | 4 |
_aLearning Disabilities _xpathology |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aTelomere _xgenetics |
| 700 | 1 | _aGupta, S | |
| 700 | 1 | _aEnoch, S | |
| 700 | 1 | _aThompson, P | |
| 700 | 1 | _aRowbottom, A | |
| 700 | 1 | _aChua, I | |
| 700 | 1 | _aWarren, S | |
| 700 | 1 | _aJohnson, D | |
| 700 | 1 | _aLedbetter, D H | |
| 700 | 1 | _aLese-Martin, C | |
| 700 | 1 | _aWilliams, P | |
| 700 | 1 | _aPilz, D T | |
| 773 | 0 |
_tAmerican journal of medical genetics. Part A _gvol. 136 _gno. 1 _gp. 38-44 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/ajmg.a.30774 _zAvailable from publisher's website |
| 999 |
_c15598211 _d15598211 |
||