| 000 | 01002 a2200313 4500 | ||
|---|---|---|---|
| 005 | 20250512120102.0 | ||
| 264 | 0 | _c19730129 | |
| 008 | 197301s 0 0 eng d | ||
| 022 | _a0018-7348 | ||
| 024 | 7 |
_a10.1007/BF00281740 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aSubrt, I | |
| 245 | 0 | 0 |
_aFurther observations on a previously reported case of 4p--syndrome. _h[electronic resource] |
| 260 |
_bHumangenetik _c1972 |
||
| 300 |
_a361-3 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xgenetics |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChromosome Aberrations |
| 650 | 0 | 4 | _aChromosome Disorders |
| 650 | 0 | 4 | _aChromosomes, Human, 4-5 |
| 650 | 0 | 4 |
_aCri-du-Chat Syndrome _xgenetics |
| 650 | 0 | 4 | _aFluorescence |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 700 | 1 | _aBlehová, B | |
| 773 | 0 |
_tHumangenetik _gvol. 15 _gno. 4 _gp. 361-3 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/BF00281740 _zAvailable from publisher's website |
| 999 |
_c4638264 _d4638264 |
||