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The author names and affiliations were published incorrectly; the correct version is as follows:
Pia Huusko1,2,11, Suh-Hang Hank Juo3,4,11, Elizabeth Gillanders1,11, Laura Sarantaus5,11, Tommi Kainu1, Pia Vahteristo5, Minna Allinen2, MaryPat Jones1, Katrin Rapakko2, Hannaleena Eerola5,6, Carol Markey1, Paula Vehmanen5, Derek Gildea1, Diane Freas-Lutz1, Carl Blomqvist6, Jaakko Leisti2, Guillermo Blanco7, Ulla Puistola8, Jeffrey Trent9, Joan Bailey-Wilson3, Robert Winqvist2, Heli Nevanlinna5 and Olli-P Kallioniemi*,9,10
1Cancer Genetics Branch, NHGRI, NIH, Bethesda, MD, USA; 2Department of Clinical Genetics, Oulu University Hospital, Oulu, Finland; 3Inherited Disease Research Branch, NHGRI, NIH, Baltimore, MD, USA; 4Columbia Genome Center, New York, NY, USA; 5Department of Obstetrics and Gynecology, Helsinki University Central Hospital, Helsinki, Finland; 6Department of Oncology, Helsinki University Central Hospital, Helsinki, Finland; 7Department of Oncology, Oulu University Hospital, Oulu, Finland; 8Department of Obstetrics and Gynecology, Oulu University Hospital, Oulu, Finland; 9Translational Genomics Research Institute, Phoenix, AZ, USA; 10VTT Technical Research Centre of Finland, Turku, Finland
In the Materials and methods; Genotyping section; a sentence was published incorrectly, the correct text is as follows:
‘For fine mapping, an additional set of 34 markers, spanning a 40 cM chromosomal region from 2q24 to 2q33, was used (Figure 2) (www.marshfieldclinic.org).’
In the Acknowledgements section, the following acknowledgement was missing: Helsingin Sanomat Foundation.
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The online version of the original article can be found at 10.1038/sj.ejhg.5201091
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Huusko, P., Juo, SH., Gillanders, E. et al. Erratum: Genome-wide scanning for linkage in Finnish breast cancer families. Eur J Hum Genet 12, 256 (2004). https://doi.org/10.1038/sj.ejhg.5201140
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DOI: https://doi.org/10.1038/sj.ejhg.5201140