000 01389 a2200421 4500
005 20250514234516.0
264 0 _c20060629
008 200606s 0 0 eng d
022 _a0197-3851
024 7 _a10.1002/pd.1193
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMøller, Lisbeth Birk
245 0 0 _aPre- and postnatal diagnosis of tyrosine hydroxylase deficiency.
_h[electronic resource]
260 _bPrenatal diagnosis
_cAug 2005
300 _a671-5 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aBrain Diseases, Metabolic, Inborn
_xdiagnosis
650 0 4 _aChild, Preschool
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aMuscle Hypotonia
_xdiagnosis
650 0 4 _aMutation
650 0 4 _aPolymerase Chain Reaction
650 0 4 _aPolymorphism, Genetic
_xgenetics
650 0 4 _aPregnancy
650 0 4 _aPrenatal Diagnosis
650 0 4 _aTyrosine 3-Monooxygenase
_xdeficiency
700 1 _aRomstad, Anne
700 1 _aPaulsen, Marianne
700 1 _aHougaard, Pia
700 1 _aOrmazabal, Aida
700 1 _aPineda, Mercé
700 1 _aBlau, Nenad
700 1 _aGüttler, Flemming
700 1 _aArtuch, Rafael
773 0 _tPrenatal diagnosis
_gvol. 25
_gno. 8
_gp. 671-5
856 4 0 _uhttps://doi.org/10.1002/pd.1193
_zAvailable from publisher's website
999 _c15703428
_d15703428