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Updated: Aug 2, 2026

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
05:51

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia

Published on: June 15, 2011

Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome

N C M Hearle, M F Rudd, W Lim

    Journal of Medical Genetics
    |April 4, 2006
    PubMed
    Abstract

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