000 | 01874 a2200529 4500 | ||
---|---|---|---|
005 | 20250513104954.0 | ||
264 | 0 | _c19970227 | |
008 | 199702s 0 0 eng d | ||
022 | _a0197-3851 | ||
024 | 7 |
_a10.1002/(SICI)1097-0223(199610)16:10<958::AID-PD971>3.0.CO;2-U _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aWebb, A L | |
245 | 0 | 0 |
_aMaternal uniparental disomy for chromosome 2 in association with confined placental mosaicism for trisomy 2 and severe intrauterine growth retardation. _h[electronic resource] |
260 |
_bPrenatal diagnosis _cOct 1996 |
||
300 |
_a958-62 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 | _aAdult |
650 | 0 | 4 |
_aAmniocentesis _xadverse effects |
650 | 0 | 4 |
_aChorionic Villi Sampling _xadverse effects |
650 | 0 | 4 | _aChromosome Aberrations |
650 | 0 | 4 | _aChromosomes, Human, Pair 2 |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 |
_aFetal Growth Retardation _xgenetics |
650 | 0 | 4 |
_aFetal Membranes, Premature Rupture _xdiagnosis |
650 | 0 | 4 | _aFundoplication |
650 | 0 | 4 | _aGestational Age |
650 | 0 | 4 |
_aHernia, Hiatal _xsurgery |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aInfant, Newborn |
650 | 0 | 4 | _aKaryotyping |
650 | 0 | 4 | _aMaternal Age |
650 | 0 | 4 | _aMosaicism |
650 | 0 | 4 | _aPlacenta |
650 | 0 | 4 | _aPregnancy |
650 | 0 | 4 | _aPregnancy, High-Risk |
650 | 0 | 4 |
_aPyloric Stenosis _xcongenital |
650 | 0 | 4 |
_aRenal Insufficiency _xdiagnosis |
650 | 0 | 4 | _aTrisomy |
650 | 0 | 4 | _aUltrasonography, Prenatal |
700 | 1 | _aSturgiss, S | |
700 | 1 | _aWarwicker, P | |
700 | 1 | _aRobson, S C | |
700 | 1 | _aGoodship, J A | |
700 | 1 | _aWolstenholme, J | |
773 | 0 |
_tPrenatal diagnosis _gvol. 16 _gno. 10 _gp. 958-62 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1002/(SICI)1097-0223(199610)16:10<958::AID-PD971>3.0.CO;2-U _zAvailable from publisher's website |
999 |
_c8930471 _d8930471 |