000 01573 a2200469 4500
005 20250516190818.0
264 0 _c20141204
008 201412s 0 0 eng d
022 _a1097-0223
024 7 _a10.1002/pd.4312
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBuysse, Karen
245 0 0 _aDetecting fetal subchromosomal aberrations by MPS: an unexpected discrepancy between amniocyte DNA and ccffDNA.
_h[electronic resource]
260 _bPrenatal diagnosis
_cApr 2014
300 _a402-5 p.
_bdigital
500 _aPublication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't
650 0 4 _aAdult
650 0 4 _aAmniocentesis
_xmethods
650 0 4 _aChromosomes, Human, Pair 13
_xgenetics
650 0 4 _aDNA
_xanalysis
650 0 4 _aFemale
650 0 4 _aFetus
_xchemistry
650 0 4 _aGene Deletion
650 0 4 _aHigh-Throughput Nucleotide Sequencing
_xmethods
650 0 4 _aHoloprosencephaly
_xgenetics
650 0 4 _aHumans
650 0 4 _aNuclear Proteins
_xgenetics
650 0 4 _aPregnancy
650 0 4 _aTranscription Factors
_xgenetics
700 1 _ade Ligt, Joep
700 1 _aJanssen, Irene M
700 1 _avan Bon, Bregje W M
700 1 _aGomes, Ingrid
700 1 _aHehir-Kwa, Jayne
700 1 _aEggink, Alex J
700 1 _avan Vugt, John M G
700 1 _aVissers, Lisenka E L M
700 1 _aGeurts van Kessel, Ad
700 1 _aFaas, Brigitte H W
773 0 _tPrenatal diagnosis
_gvol. 34
_gno. 4
_gp. 402-5
856 4 0 _uhttps://doi.org/10.1002/pd.4312
_zAvailable from publisher's website
999 _c23417771
_d23417771