000 01441 a2200421 4500
005 20250516115920.0
264 0 _c20130430
008 201304s 0 0 eng d
022 _a1097-0223
024 7 _a10.1002/pd.3986
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMann, Kathy
245 0 0 _aQuantitative fluorescence PCR analysis of >40,000 prenatal samples for the rapid diagnosis of trisomies 13, 18 and 21 and monosomy X.
_h[electronic resource]
260 _bPrenatal diagnosis
_cDec 2012
300 _a1197-204 p.
_bdigital
500 _aPublication Type: Evaluation Study; Journal Article
650 0 4 _aChromosomes, Human, Pair 13
650 0 4 _aChromosomes, Human, Pair 18
650 0 4 _aChromosomes, Human, Pair 21
650 0 4 _aChromosomes, Human, X
650 0 4 _aFemale
650 0 4 _aFluorescence
650 0 4 _aHumans
650 0 4 _aMonosomy
_xdiagnosis
650 0 4 _aPolymerase Chain Reaction
_xmethods
650 0 4 _aPregnancy
650 0 4 _aPrenatal Diagnosis
_xmethods
650 0 4 _aRetrospective Studies
650 0 4 _aSex Chromosome Aberrations
650 0 4 _aTime Factors
650 0 4 _aTrisomy
_xdiagnosis
700 1 _aHills, Alison
700 1 _aDonaghue, Celia
700 1 _aThomas, Helen
700 1 _aOgilvie, Caroline Mackie
773 0 _tPrenatal diagnosis
_gvol. 32
_gno. 12
_gp. 1197-204
856 4 0 _uhttps://doi.org/10.1002/pd.3986
_zAvailable from publisher's website
999 _c22211765
_d22211765