| 000 | 01555 a2200517 4500 | ||
|---|---|---|---|
| 005 | 20250517223550.0 | ||
| 264 | 0 | _c20191028 | |
| 008 | 201910s 0 0 eng d | ||
| 022 | _a1399-0004 | ||
| 024 | 7 |
_a10.1111/cge.13409 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aBrischoux-Boucher, E | |
| 245 | 0 | 0 |
_aIL11RA-related Crouzon-like autosomal recessive craniosynostosis in 10 new patients: Resemblances and differences. _h[electronic resource] |
| 260 |
_bClinical genetics _c10 2018 |
||
| 300 |
_a373-380 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 |
_aCraniofacial Dysostosis _xdiagnostic imaging |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenes, Recessive |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aInterleukin-11 Receptor alpha Subunit _xgenetics |
| 650 | 0 | 4 | _aMagnetic Resonance Imaging |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMutation, Missense |
| 700 | 1 | _aTrimouille, A | |
| 700 | 1 | _aBaujat, G | |
| 700 | 1 | _aGoldenberg, A | |
| 700 | 1 | _aSchaefer, E | |
| 700 | 1 | _aGuichard, B | |
| 700 | 1 | _aHannequin, P | |
| 700 | 1 | _aPaternoster, G | |
| 700 | 1 | _aBaer, S | |
| 700 | 1 | _aCabrol, C | |
| 700 | 1 | _aWeber, E | |
| 700 | 1 | _aGodfrin, G | |
| 700 | 1 | _aLenoir, M | |
| 700 | 1 | _aLacombe, D | |
| 700 | 1 | _aCollet, C | |
| 700 | 1 | _aVan Maldergem, L | |
| 773 | 0 |
_tClinical genetics _gvol. 94 _gno. 3-4 _gp. 373-380 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/cge.13409 _zAvailable from publisher's website |
| 999 |
_c28553660 _d28553660 |
||