000 01314 a2200409 4500
005 20250515053235.0
264 0 _c20071106
008 200711s 0 0 eng d
022 _a1750-1172
024 7 _a10.1186/1750-1172-2-4
_2doi
040 _aNLM
_beng
_cNLM
100 1 _avan der Burgt, Ineke
245 0 0 _aNoonan syndrome.
_h[electronic resource]
260 _bOrphanet journal of rare diseases
_cJan 2007
300 _a4 p.
_bdigital
500 _aPublication Type: Journal Article; Review
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aChild
650 0 4 _aChild Development
650 0 4 _aChild, Preschool
650 0 4 _aFemale
650 0 4 _aGenetic Counseling
_xmethods
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aInfant, Newborn
650 0 4 _aIntracellular Signaling Peptides and Proteins
_xgenetics
650 0 4 _aMutation, Missense
650 0 4 _aNoonan Syndrome
_xdiagnosis
650 0 4 _aPregnancy
650 0 4 _aPrenatal Diagnosis
_xmethods
650 0 4 _aPrognosis
650 0 4 _aProtein Tyrosine Phosphatase, Non-Receptor Type 11
650 0 4 _aProtein Tyrosine Phosphatases
_xgenetics
773 0 _tOrphanet journal of rare diseases
_gvol. 2
_gp. 4
856 4 0 _uhttps://doi.org/10.1186/1750-1172-2-4
_zAvailable from publisher's website
999 _c16787152
_d16787152