000 01171 a2200349 4500
005 20250518002752.0
264 0 _c20190304
008 201903s 0 0 fre d
022 _a2468-7189
024 7 _a10.1016/j.gofs.2018.09.010
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSchaub, M
245 0 0 _a[Prenatal diagnosis of Prader-Willi syndrome with CGH-Array: About a case].
_h[electronic resource]
260 _bGynecologie, obstetrique, fertilite & senologie
_c11 2018
300 _a747-749 p.
_bdigital
500 _aPublication Type: Case Reports; Letter
650 0 4 _aAdult
650 0 4 _aChromosomes, Human, Pair 15
650 0 4 _aFemale
650 0 4 _aGene Deletion
650 0 4 _aGestational Age
650 0 4 _aHumans
650 0 4 _aPrader-Willi Syndrome
_xdiagnosis
650 0 4 _aPregnancy
650 0 4 _aPrenatal Diagnosis
_xmethods
700 1 _aViville, B
700 1 _aGirard, F
700 1 _aEl Chehadeh, S
700 1 _aLanger, B
773 0 _tGynecologie, obstetrique, fertilite & senologie
_gvol. 46
_gno. 10-11
_gp. 747-749
856 4 0 _uhttps://doi.org/10.1016/j.gofs.2018.09.010
_zAvailable from publisher's website
999 _c28934844
_d28934844