| 000 | 01071 a2200361 4500 | ||
|---|---|---|---|
| 005 | 20250512234846.0 | ||
| 264 | 0 | _c19830729 | |
| 008 | 198307s 0 0 eng d | ||
| 022 | _a0340-6717 | ||
| 024 | 7 |
_a10.1007/BF00284669 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aStoll, C | |
| 245 | 0 | 0 |
_aSegregation of a 22 ring chromosome in three generations. _h[electronic resource] |
| 260 |
_bHuman genetics _c1983 |
||
| 300 |
_a294-6 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aChild, Preschool |
| 650 | 0 | 4 | _aChromosome Aberrations |
| 650 | 0 | 4 | _aChromosomes, Human, 21-22 and Y |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMeiosis |
| 650 | 0 | 4 | _aMosaicism |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aSyndrome |
| 700 | 1 | _aRoth, M P | |
| 773 | 0 |
_tHuman genetics _gvol. 63 _gno. 3 _gp. 294-6 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/BF00284669 _zAvailable from publisher's website |
| 999 |
_c6852560 _d6852560 |
||