000 01197 a2200349 4500
005 20250516094402.0
264 0 _c20130116
008 201301s 0 0 eng d
022 _a1473-5717
024 7 _a10.1097/MCD.0b013e3283557231
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aCroonen, Ellen A
245 0 0 _aPatient with a neurofibromatosis type 1 mutation but a clinical diagnosis of Noonan syndrome.
_h[electronic resource]
260 _bClinical dysmorphology
_cOct 2012
300 _a212-214 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aDiagnosis, Differential
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aInfant, Newborn
650 0 4 _aMutation
_xgenetics
650 0 4 _aNeurofibromatosis 1
_xgenetics
650 0 4 _aNoonan Syndrome
_xdiagnosis
700 1 _aYntema, Helger G
700 1 _avan Minkelen, Rick
700 1 _avan den Ouweland, Ans M W
700 1 _avan der Burgt, Ineke
773 0 _tClinical dysmorphology
_gvol. 21
_gno. 4
_gp. 212-214
856 4 0 _uhttps://doi.org/10.1097/MCD.0b013e3283557231
_zAvailable from publisher's website
999 _c21835512
_d21835512