000 | 01252 a2200385 4500 | ||
---|---|---|---|
005 | 20250513151651.0 | ||
264 | 0 | _c19981103 | |
008 | 199811s 0 0 eng d | ||
022 | _a0009-9163 | ||
024 | 7 |
_a10.1111/j.1399-0004.1998.tb03696.x _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aMagee, A C | |
245 | 0 | 0 |
_aDe novo direct duplication 2 (p12-->p21) with paternally inherited pericentric inversion 2p11.2 2q12.2. _h[electronic resource] |
260 |
_bClinical genetics _cJul 1998 |
||
300 |
_a65-9 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article | ||
650 | 0 | 4 |
_aAbnormalities, Multiple _xgenetics |
650 | 0 | 4 | _aAdult |
650 | 0 | 4 | _aChild, Preschool |
650 | 0 | 4 | _aChromosome Aberrations |
650 | 0 | 4 | _aChromosome Banding |
650 | 0 | 4 | _aChromosome Disorders |
650 | 0 | 4 | _aChromosome Inversion |
650 | 0 | 4 | _aChromosomes, Human, Pair 2 |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aKaryotyping |
650 | 0 | 4 | _aMale |
700 | 1 | _aHumphreys, M W | |
700 | 1 | _aMcKee, S | |
700 | 1 | _aStewart, M | |
700 | 1 | _aNevin, N C | |
773 | 0 |
_tClinical genetics _gvol. 54 _gno. 1 _gp. 65-9 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1111/j.1399-0004.1998.tb03696.x _zAvailable from publisher's website |
999 |
_c9692936 _d9692936 |