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