| 000 | 01396 a2200397 4500 | ||
|---|---|---|---|
| 005 | 20250516181428.0 | ||
| 264 | 0 | _c20140717 | |
| 008 | 201407s 0 0 eng d | ||
| 022 | _a1750-1172 | ||
| 024 | 7 |
_a10.1186/1750-1172-8-178 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aFarag, Heba Gamal | |
| 245 | 0 | 0 |
_aAbnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation. _h[electronic resource] |
| 260 |
_bOrphanet journal of rare diseases _cNov 2013 |
||
| 300 |
_a178 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aCell Cycle Proteins |
| 650 | 0 | 4 |
_aCentrosome _xmetabolism |
| 650 | 0 | 4 | _aHeterozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMicrocephaly |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aNerve Tissue Proteins _xgenetics |
| 650 | 0 | 4 |
_aSpindle Apparatus _xmetabolism |
| 700 | 1 | _aFroehler, Sebastian | |
| 700 | 1 | _aOexle, Konrad | |
| 700 | 1 | _aRavindran, Ethiraj | |
| 700 | 1 | _aSchindler, Detlev | |
| 700 | 1 | _aStaab, Timo | |
| 700 | 1 | _aHuebner, Angela | |
| 700 | 1 | _aKraemer, Nadine | |
| 700 | 1 | _aChen, Wei | |
| 700 | 1 | _aKaindl, Angela M | |
| 773 | 0 |
_tOrphanet journal of rare diseases _gvol. 8 _gp. 178 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1186/1750-1172-8-178 _zAvailable from publisher's website |
| 999 |
_c23264334 _d23264334 |
||