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A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
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Phenylketonuria and hyperphenylalaninemia in eastern Germany: a characteristic molecular profile and 15 novel

J B Hennermann1, B Vetter, C Wolf

  • 1Children's Hospital, Charité Medical Center, Humboldt University, Berlin, Germany.

Human Mutation
|February 19, 2000
PubMed

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