| 000 | 01091 a2200313 4500 | ||
|---|---|---|---|
| 005 | 20250517001213.0 | ||
| 264 | 0 | _c20150521 | |
| 008 | 201505s 0 0 eng d | ||
| 022 | _a1552-4833 | ||
| 024 | 7 |
_a10.1002/ajmg.a.36797 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aHancarova, Miroslava | |
| 245 | 0 | 0 |
_aDeletions of 9q21.3 including NTRK2 are associated with severe phenotype. _h[electronic resource] |
| 260 |
_bAmerican journal of medical genetics. Part A _cJan 2015 |
||
| 300 |
_a264-7 p. _bdigital |
||
| 500 | _aPublication Type: Letter; Comment | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xdiagnosis |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 | _aChromosomes, Human, Pair 9 |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 700 | 1 | _aPuchmajerova, Alena | |
| 700 | 1 | _aDrabova, Jana | |
| 700 | 1 | _aKaraskova, Eliska | |
| 700 | 1 | _aVlckova, Marketa | |
| 700 | 1 | _aSedlacek, Zdenek | |
| 773 | 0 |
_tAmerican journal of medical genetics. Part A _gvol. 167A _gno. 1 _gp. 264-7 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/ajmg.a.36797 _zAvailable from publisher's website |
| 999 |
_c24309241 _d24309241 |
||