| 000 | 01231 a2200337 4500 | ||
|---|---|---|---|
| 005 | 20250518041106.0 | ||
| 264 | 0 | _c20190904 | |
| 008 | 201909s 0 0 eng d | ||
| 022 | _a1878-0849 | ||
| 024 | 7 |
_a10.1016/j.ejmg.2019.103671 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aEggermann, Thomas | |
| 245 | 0 | 0 |
_aContribution of GRB10 to the prenatal phenotype in Silver-Russell syndrome? Lessons from 7p12 copy number variations. _h[electronic resource] |
| 260 |
_bEuropean journal of medical genetics _cJul 2019 |
||
| 300 |
_a103671 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 7 _xgenetics |
| 650 | 0 | 4 | _aDNA Copy Number Variations |
| 650 | 0 | 4 |
_aFetal Development _xgenetics |
| 650 | 0 | 4 |
_aGRB10 Adaptor Protein _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aSilver-Russell Syndrome _xgenetics |
| 700 | 1 | _aBegemann, Matthias | |
| 700 | 1 | _aKurth, Ingo | |
| 700 | 1 | _aElbracht, Miriam | |
| 773 | 0 |
_tEuropean journal of medical genetics _gvol. 62 _gno. 7 _gp. 103671 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.ejmg.2019.103671 _zAvailable from publisher's website |
| 999 |
_c29701716 _d29701716 |
||