Pre- and postnatal diagnosis of tyrosine hydroxylase deficiency.
Møller, Lisbeth Birk
Pre- and postnatal diagnosis of tyrosine hydroxylase deficiency. [electronic resource] - Prenatal diagnosis Aug 2005 - 671-5 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
0197-3851
10.1002/pd.1193 doi
Brain Diseases, Metabolic, Inborn--diagnosis
Child, Preschool
Female
Humans
Muscle Hypotonia--diagnosis
Mutation
Polymerase Chain Reaction
Polymorphism, Genetic--genetics
Pregnancy
Prenatal Diagnosis
Tyrosine 3-Monooxygenase--deficiency
Pre- and postnatal diagnosis of tyrosine hydroxylase deficiency. [electronic resource] - Prenatal diagnosis Aug 2005 - 671-5 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
0197-3851
10.1002/pd.1193 doi
Brain Diseases, Metabolic, Inborn--diagnosis
Child, Preschool
Female
Humans
Muscle Hypotonia--diagnosis
Mutation
Polymerase Chain Reaction
Polymorphism, Genetic--genetics
Pregnancy
Prenatal Diagnosis
Tyrosine 3-Monooxygenase--deficiency