| 000 | 01266 a2200397 4500 | ||
|---|---|---|---|
| 005 | 20250511170806.0 | ||
| 264 | 0 | _c19751105 | |
| 008 | 197511s 0 0 eng d | ||
| 022 | _a0018-7348 | ||
| 024 | 7 |
_a10.1007/BF00278357 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aStoll, C | |
| 245 | 0 | 0 |
_aBalanced familial translocation t(5;19)(q12;p or q11) with phenotypical abnormalities in a girl. _h[electronic resource] |
| 260 |
_bHumangenetik _c1975 |
||
| 300 |
_a263-7 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 |
_aCarotid Arteries _xabnormalities |
| 650 | 0 | 4 | _aChild |
| 650 | 0 | 4 | _aChromosome Aberrations |
| 650 | 0 | 4 | _aChromosomes, Human, 19-20 |
| 650 | 0 | 4 | _aChromosomes, Human, 4-5 |
| 650 | 0 | 4 | _aChromosomes, Human, 6-12 and X |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aKaryotyping |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aPrognathism _xgenetics |
| 650 | 0 | 4 | _aTranslocation, Genetic |
| 650 | 0 | 4 |
_aUrinary Tract _xabnormalities |
| 650 | 0 | 4 |
_aVision Disorders _xgenetics |
| 700 | 1 | _aLevy, J M | |
| 700 | 1 | _aChampy, M | |
| 773 | 0 |
_tHumangenetik _gvol. 27 _gno. 3 _gp. 263-7 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/BF00278357 _zAvailable from publisher's website |
| 999 |
_c1156931 _d1156931 |
||