| 000 | 00889 a2200277 4500 | ||
|---|---|---|---|
| 005 | 20250511134015.0 | ||
| 264 | 0 | _c19791024 | |
| 008 | 197910s 0 0 eng d | ||
| 022 | _a0340-6717 | ||
| 024 | 7 |
_a10.1007/BF00295597 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aPetit, P | |
| 245 | 0 | 0 |
_aA chromosomal abnormality (21q-) in primary thrombocytosis. _h[electronic resource] |
| 260 |
_bHuman genetics _c1979 |
||
| 300 |
_a105-6 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 | _aAged |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 | _aChromosomes, Human, 21-22 and Y |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aThrombocytosis _xgenetics |
| 700 | 1 | _aVan den Berghe, H | |
| 773 | 0 |
_tHuman genetics _gvol. 50 _gno. 1 _gp. 105-6 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/BF00295597 _zAvailable from publisher's website |
| 999 |
_c488684 _d488684 |
||