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  1. Article

    Erratum: Sensitive mutation detection in heterogeneous cancer specimens by massively parallel picoliter reactor sequencing

    Nat. Med. 12, 852–855 (2006); published online 25 June; corrected after print 13 September 2006 In the version of this article initially published, it should have been acknowledged that Jan F. Simons, in addit...

    R K Thomas, E Nickerson, J F Simons, P A Jänne, T Tengs, Y Yuza… in Nature Medicine (2006)

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    Article

    Maternal but not paternal transmission of 15q11–13–linked nondeletion Angelman syndrome leads to phenotypic expression

    Angelman syndrome (AS) may result from either maternally inherited deletions of chromosome 15q11–13 or from paternal uniparental disomy for chromosome 15. This is in contrast to Prader–Willi syndrome (PWS), wh...

    J. Wagstaff, J.H.M. Knoll, K.A. Glatt, Y.Y. Shugart, A. Sommer… in Nature Genetics (1992)