| 000 | 01367 a2200385 4500 | ||
|---|---|---|---|
| 005 | 20250513013649.0 | ||
| 264 | 0 | _c19810521 | |
| 008 | 198105s 0 0 eng d | ||
| 022 | _a0148-7299 | ||
| 024 | 7 |
_a10.1002/ajmg.1320070412 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aZackai, E H | |
| 245 | 0 | 0 |
_aSite-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction. _h[electronic resource] |
| 260 |
_bAmerican journal of medical genetics _c1980 |
||
| 300 |
_a507-21 p. _bdigital |
||
| 500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. | ||
| 650 | 0 | 4 |
_aAbnormalities, Multiple _xgenetics |
| 650 | 0 | 4 | _aChromosomes, Human, 21-22 and Y |
| 650 | 0 | 4 | _aChromosomes, Human, 6-12 and X |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aInfant, Newborn |
| 650 | 0 | 4 |
_aIntellectual Disability _xgenetics |
| 650 | 0 | 4 | _aKaryotyping |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMeiosis |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aTranslocation, Genetic |
| 650 | 0 | 4 | _aTrisomy |
| 700 | 1 | _aEmanuel, B S | |
| 773 | 0 |
_tAmerican journal of medical genetics _gvol. 7 _gno. 4 _gp. 507-21 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/ajmg.1320070412 _zAvailable from publisher's website |
| 999 |
_c7211484 _d7211484 |
||