000 | 00898 a2200289 4500 | ||
---|---|---|---|
005 | 20250512170733.0 | ||
264 | 0 | _c19680710 | |
008 | 196807s 0 0 eng d | ||
022 | _a0018-0661 | ||
024 | 7 |
_a10.1111/j.1601-5223.1967.tb02118.x _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aHall, B | |
245 | 0 | 0 |
_aA case of monosomy G? _h[electronic resource] |
260 |
_bHereditas _c1967 |
||
300 |
_a356-64 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article | ||
650 | 0 | 4 | _aChromosome Aberrations |
650 | 0 | 4 | _aChromosome Disorders |
650 | 0 | 4 | _aChromosomes, Human, 21-22 and Y |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aInfant |
650 | 0 | 4 | _aMale |
700 | 1 | _aFredga, K | |
700 | 1 | _aSvenningsen, N | |
773 | 0 |
_tHereditas _gvol. 57 _gno. 3 _gp. 356-64 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1111/j.1601-5223.1967.tb02118.x _zAvailable from publisher's website |
999 |
_c5587979 _d5587979 |