| 000 | 01558 a2200469 4500 | ||
|---|---|---|---|
| 005 | 20250513115858.0 | ||
| 264 | 0 | _c19970509 | |
| 008 | 199705s 0 0 eng d | ||
| 022 | _a0009-9163 | ||
| 024 | 7 |
_a10.1111/j.1399-0004.1996.tb02725.x _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aPetković, I | |
| 245 | 0 | 0 |
_aUnusual segregation of t(11;22) resulting from crossing-over followed by 3:1 disjunction at meiosis I. _h[electronic resource] |
| 260 |
_bClinical genetics _cDec 1996 |
||
| 300 |
_a515-9 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xgenetics |
| 650 | 0 | 4 | _aAnaphase |
| 650 | 0 | 4 | _aAneuploidy |
| 650 | 0 | 4 |
_aChromosome Aberrations _xgenetics |
| 650 | 0 | 4 | _aChromosome Disorders |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 11 _xgenetics |
| 650 | 0 | 4 |
_aChromosomes, Human, Pair 22 _xgenetics |
| 650 | 0 | 4 | _aCrossing Over, Genetic |
| 650 | 0 | 4 |
_aFace _xabnormalities |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
| 650 | 0 | 4 | _aKaryotyping |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMuscle Hypotonia _xgenetics |
| 650 | 0 | 4 | _aNondisjunction, Genetic |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aSpermatogenesis |
| 650 | 0 | 4 | _aTranslocation, Genetic |
| 700 | 1 | _ade Capoa, A | |
| 700 | 1 | _aGiancotti, P | |
| 700 | 1 | _aBarisić, I | |
| 773 | 0 |
_tClinical genetics _gvol. 50 _gno. 6 _gp. 515-9 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/j.1399-0004.1996.tb02725.x _zAvailable from publisher's website |
| 999 |
_c9129252 _d9129252 |
||