| 000 | 01078 a2200337 4500 | ||
|---|---|---|---|
| 005 | 20250512233222.0 | ||
| 264 | 0 | _c19820412 | |
| 008 | 198204s 0 0 eng d | ||
| 022 | _a0003-3995 | ||
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aMüller, U | |
| 245 | 0 | 0 |
_aA patient with interstitial deletion 7 (p13 leads to p21). _h[electronic resource] |
| 260 |
_bAnnales de genetique _c1981 |
||
| 300 |
_a239-41 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xgenetics |
| 650 | 0 | 4 |
_aChromosome Aberrations _xgenetics |
| 650 | 0 | 4 | _aChromosome Deletion |
| 650 | 0 | 4 | _aChromosome Disorders |
| 650 | 0 | 4 | _aChromosomes, Human, 6-12 and X |
| 650 | 0 | 4 |
_aEpilepsy, Tonic-Clonic _xgenetics |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 |
_aHeart Septal Defects, Atrial _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 |
_aSkull _xabnormalities |
| 650 | 0 | 4 | _aUrogenital Abnormalities |
| 700 | 1 | _aStaudt, F | |
| 700 | 1 | _aHameister, H | |
| 773 | 0 |
_tAnnales de genetique _gvol. 24 _gno. 4 _gp. 239-41 |
|
| 999 |
_c6800046 _d6800046 |
||