| 000 | 01159 a2200349 4500 | ||
|---|---|---|---|
| 005 | 20250515033410.0 | ||
| 264 | 0 | _c20070220 | |
| 008 | 200702s 0 0 eng d | ||
| 022 | _a1552-4825 | ||
| 024 | 7 |
_a10.1002/ajmg.a.31346 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aHennekam, Raoul C M | |
| 245 | 0 | 0 |
_aHutchinson-Gilford progeria syndrome: review of the phenotype. _h[electronic resource] |
| 260 |
_bAmerican journal of medical genetics. Part A _cDec 2006 |
||
| 300 |
_a2603-24 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Review | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xdiagnosis |
| 650 | 0 | 4 |
_aCardiovascular Diseases _xpathology |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 |
_aLamin Type A _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aModels, Genetic |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aOsteolysis _xpathology |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aProgeria _xdiagnosis |
| 773 | 0 |
_tAmerican journal of medical genetics. Part A _gvol. 140 _gno. 23 _gp. 2603-24 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/ajmg.a.31346 _zAvailable from publisher's website |
| 999 |
_c16429305 _d16429305 |
||