LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome

[electronic letter]

E Volikos, J Robinson, Kristiina Aittomäki, Jukka-Pekka Mecklin, Heikki Järvinen, A. M Westerman, F. W. M de Rooij, T Vogel, G Moeslein, Virpi Launonen, I. P. M Tomlinson, A. R. J Silver, Lauri A Aaltonen

    Research output: Contribution to journalArticleScientificpeer-review

    Original languageEnglish
    JournalJournal of Medical Genetics
    Volume43
    Issue number5
    Pages (from-to)e18
    Number of pages3
    ISSN0022-2593
    DOIs
    Publication statusPublished - 2006
    MoE publication typeA1 Journal article-refereed

    Fields of Science

    • 311 Basic medicine

    Cite this

    Volikos, E ; Robinson, J ; Aittomäki, Kristiina ; Mecklin, Jukka-Pekka ; Järvinen, Heikki ; Westerman, A. M ; de Rooij, F. W. M ; Vogel, T ; Moeslein, G ; Launonen, Virpi ; Tomlinson, I. P. M ; Silver, A. R. J ; Aaltonen, Lauri A. / LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome : [electronic letter]. In: Journal of Medical Genetics. 2006 ; Vol. 43, No. 5. pp. e18.
    @article{55dc35bf061c4095a6b7301c8fb55770,
    title = "LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome: [electronic letter]",
    keywords = "311 Basic medicine",
    author = "E Volikos and J Robinson and Kristiina Aittom{\"a}ki and Jukka-Pekka Mecklin and Heikki J{\"a}rvinen and Westerman, {A. M} and {de Rooij}, {F. W. M} and T Vogel and G Moeslein and Virpi Launonen and Tomlinson, {I. P. M} and Silver, {A. R. J} and Aaltonen, {Lauri A}",
    year = "2006",
    doi = "10.1136/jmg.2005.039875",
    language = "English",
    volume = "43",
    pages = "e18",
    journal = "Journal of Medical Genetics",
    issn = "0022-2593",
    publisher = "BMJ Publishing Group Ltd",
    number = "5",

    }

    Volikos, E, Robinson, J, Aittomäki, K, Mecklin, J-P, Järvinen, H, Westerman, AM, de Rooij, FWM, Vogel, T, Moeslein, G, Launonen, V, Tomlinson, IPM, Silver, ARJ & Aaltonen, LA 2006, 'LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome: [electronic letter]', Journal of Medical Genetics, vol. 43, no. 5, pp. e18. https://doi.org/10.1136/jmg.2005.039875

    LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome : [electronic letter]. / Volikos, E; Robinson, J; Aittomäki, Kristiina; Mecklin, Jukka-Pekka; Järvinen, Heikki; Westerman, A. M; de Rooij, F. W. M; Vogel, T; Moeslein, G; Launonen, Virpi; Tomlinson, I. P. M; Silver, A. R. J; Aaltonen, Lauri A.

    In: Journal of Medical Genetics, Vol. 43, No. 5, 2006, p. e18.

    Research output: Contribution to journalArticleScientificpeer-review

    TY - JOUR

    T1 - LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome

    T2 - [electronic letter]

    AU - Volikos, E

    AU - Robinson, J

    AU - Aittomäki, Kristiina

    AU - Mecklin, Jukka-Pekka

    AU - Järvinen, Heikki

    AU - Westerman, A. M

    AU - de Rooij, F. W. M

    AU - Vogel, T

    AU - Moeslein, G

    AU - Launonen, Virpi

    AU - Tomlinson, I. P. M

    AU - Silver, A. R. J

    AU - Aaltonen, Lauri A

    PY - 2006

    Y1 - 2006

    KW - 311 Basic medicine

    U2 - 10.1136/jmg.2005.039875

    DO - 10.1136/jmg.2005.039875

    M3 - Article

    VL - 43

    SP - e18

    JO - Journal of Medical Genetics

    JF - Journal of Medical Genetics

    SN - 0022-2593

    IS - 5

    ER -