000			01543 a2200445 4500
005			20250516043705.0
264		0	_c20140121
008			201401s 0 0 eng d
022			_a1097-0223
024	7		_a10.1002/pd.2782 _2doi
040			_aNLM _beng _cNLM
100	1		_aBakker, M
245	0	0	_aTargeted ultrasound examination and DNA testing for Noonan syndrome, in fetuses with increased nuchal translucency and normal karyotype. _h[electronic resource]
260			_bPrenatal diagnosis _cSep 2011
300			_a833-40 p. _bdigital
500			_aPublication Type: Case Reports; Journal Article; Review
650	0	4	_aAdult
650	0	4	_aCraniofacial Abnormalities
650	0	4	_aDNA _xanalysis
650	0	4	_aFemale
650	0	4	_aGestational Age
650	0	4	_aHeart Defects, Congenital _xdiagnostic imaging
650	0	4	_aHumans
650	0	4	_aKaryotype
650	0	4	_aLymphangioma, Cystic _xdiagnostic imaging
650	0	4	_aMale
650	0	4	_aMutation
650	0	4	_aNoonan Syndrome _xdiagnostic imaging
650	0	4	_aNuchal Translucency Measurement
650	0	4	_aPolyhydramnios _xdiagnostic imaging
650	0	4	_aPregnancy
650	0	4	_aPrenatal Diagnosis
650	0	4	_aProtein Tyrosine Phosphatase, Non-Receptor Type 11 _xgenetics
650	0	4	_aUltrasonography, Prenatal
700	1		_aPajkrt, E
700	1		_aMathijssen, I B
700	1		_aBilardo, C M
773	0		_tPrenatal diagnosis _gvol. 31 _gno. 9 _gp. 833-40
856	4	0	_uhttps://doi.org/10.1002/pd.2782 _zAvailable from publisher's website
999			_c20960131 _d20960131