000 | 01723 a2200553 4500 | ||
---|---|---|---|
005 | 20250512142851.0 | ||
264 | 0 | _c19721226 | |
008 | 197212s 0 0 eng d | ||
022 | _a0022-2593 | ||
024 | 7 |
_a10.1136/jmg.9.3.280 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aReiss, J A | |
245 | 0 | 0 |
_aMosaicism with translocation: autoradiographic and fluorescent studies of an inherited reciprocal translocation t(2q+;14q-). _h[electronic resource] |
260 |
_bJournal of medical genetics _cSep 1972 |
||
300 |
_a280-6 p. _bdigital |
||
500 | _aPublication Type: Journal Article | ||
650 | 0 | 4 |
_aAbnormalities, Multiple _xgenetics |
650 | 0 | 4 | _aAdult |
650 | 0 | 4 | _aAneuploidy |
650 | 0 | 4 | _aAutoradiography |
650 | 0 | 4 | _aBlood Group Antigens |
650 | 0 | 4 | _aChild |
650 | 0 | 4 |
_aChromosome Aberrations _xdiagnosis |
650 | 0 | 4 | _aChromosome Disorders |
650 | 0 | 4 | _aChromosomes, Human, 1-3 |
650 | 0 | 4 | _aChromosomes, Human, 13-15 |
650 | 0 | 4 | _aCulture Techniques |
650 | 0 | 4 | _aDiagnosis, Differential |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 |
_aFibroblasts _xcytology |
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 | _aMicroscopy, Fluorescence |
650 | 0 | 4 | _aMosaicism |
650 | 0 | 4 |
_aPsychomotor Disorders _xgenetics |
650 | 0 | 4 | _aQuinacrine |
650 | 0 | 4 |
_aSkin _xcytology |
650 | 0 | 4 | _aThymidine |
650 | 0 | 4 | _aTritium |
700 | 1 | _aWyandt, H E | |
700 | 1 | _aMagenis, R E | |
700 | 1 | _aLovrien, E W | |
700 | 1 | _aHecht, F | |
773 | 0 |
_tJournal of medical genetics _gvol. 9 _gno. 3 _gp. 280-6 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1136/jmg.9.3.280 _zAvailable from publisher's website |
999 |
_c5081540 _d5081540 |