000 01403 a2200373 4500
005 20250517054629.0
264 0 _c20161028
008 201610s 0 0 eng d
022 _a1097-0223
024 7 _a10.1002/pd.4701
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aJones, Gabriela E
245 0 0 _aShould we offer prenatal testing for 17q12 microdeletion syndrome to all cases with prenatally diagnosed echogenic kidneys? Prenatal findings in two families with 17q12 microdeletion syndrome and review of the literature.
_h[electronic resource]
260 _bPrenatal diagnosis
_cDec 2015
300 _a1336-41 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Review
650 0 4 _aAbnormalities, Multiple
_xdiagnostic imaging
650 0 4 _aAdult
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 17
_xdiagnostic imaging
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aIntellectual Disability
_xdiagnostic imaging
650 0 4 _aKidney
_xdiagnostic imaging
650 0 4 _aMale
650 0 4 _aUltrasonography, Prenatal
700 1 _aMousa, Hatem A
700 1 _aRowley, Helen
700 1 _aHoutman, Peter
700 1 _aVasudevan, Pradeep C
773 0 _tPrenatal diagnosis
_gvol. 35
_gno. 13
_gp. 1336-41
856 4 0 _uhttps://doi.org/10.1002/pd.4701
_zAvailable from publisher's website
999 _c25317889
_d25317889