000 | 01796 a2200505 4500 | ||
---|---|---|---|
005 | 20250514000245.0 | ||
264 | 0 | _c20010913 | |
008 | 200109s 0 0 eng d | ||
022 | _a0148-7299 | ||
024 | 7 |
_a10.1002/1096-8628(20010501)100:3<246::aid-ajmg1254>3.0.co;2-n _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aLee, C | |
245 | 0 | 0 |
_aPrenatal diagnosis and molecular cytogenetics in a case of partial trisomy 14 and monosomy 21. _h[electronic resource] |
260 |
_bAmerican journal of medical genetics _cMay 2001 |
||
300 |
_a246-50 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 |
_aAbnormalities, Multiple _xdiagnosis |
650 | 0 | 4 | _aAdult |
650 | 0 | 4 |
_aCerebral Ventricles _xabnormalities |
650 | 0 | 4 | _aChromosomes, Human, Pair 14 |
650 | 0 | 4 | _aChromosomes, Human, Pair 21 |
650 | 0 | 4 |
_aCleft Palate _xdiagnostic imaging |
650 | 0 | 4 | _aCytogenetic Analysis |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 |
_aFetal Growth Retardation _xdiagnostic imaging |
650 | 0 | 4 |
_aFetus _xabnormalities |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 |
_aIn Situ Hybridization, Fluorescence _xmethods |
650 | 0 | 4 | _aInfant, Newborn |
650 | 0 | 4 | _aKaryotyping |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMonosomy |
650 | 0 | 4 | _aPregnancy |
650 | 0 | 4 | _aPregnancy Trimester, Second |
650 | 0 | 4 | _aTranslocation, Genetic |
650 | 0 | 4 | _aTrisomy |
650 | 0 | 4 | _aUltrasonography, Prenatal |
700 | 1 | _aFowler, D J | |
700 | 1 | _aLemyre, E | |
700 | 1 | _aSandstrom, M M | |
700 | 1 | _aHolmes, L B | |
700 | 1 | _aMorton, C C | |
773 | 0 |
_tAmerican journal of medical genetics _gvol. 100 _gno. 3 _gp. 246-50 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1002/1096-8628(20010501)100:3<246::aid-ajmg1254>3.0.co;2-n _zAvailable from publisher's website |
999 |
_c11276104 _d11276104 |