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

E Volikos; Robinson  J; Aittomaki K; Mecklin JP; Jarvinen H; Westerman AM; de Rooji FW; Vogel T; Moeslein G; Launonen V; Ian Tomlinson; Silver AR; Aaltonen LA

doi:10.1136/jmg.2005.039875

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

E Volikos, Robinson J, Aittomaki K, Mecklin JP, Jarvinen H, Westerman AM, de Rooji FW, Vogel T, Moeslein G, Launonen V, Ian Tomlinson, Silver AR, Aaltonen LA

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	e18-e18
Journal	Journal of Medical Genetics
Volume	43
Issue number	5
DOIs	https://doi.org/10.1136/jmg.2005.039875
Publication status	Published - 2006

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10.1136/jmg.2005.039875

http://jmg.bmj.com/cgi/doi/10.1136/jmg.2005.039875

Cite this

@article{1d630d4bf8ca43778e40b08fb97533ec,

title = "LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome",

author = "E Volikos and Robinson J and Aittomaki K and Mecklin JP and Jarvinen H and Westerman AM and FW, {de Rooji} and Vogel T and Moeslein G and Launonen V and Ian Tomlinson and Silver AR and Aaltonen LA",

year = "2006",

doi = "10.1136/jmg.2005.039875",

language = "English",

volume = "43",

pages = "e18--e18",

journal = "Journal of Medical Genetics",

issn = "0022-2593",

publisher = "BMJ Publishing Group",

number = "5",

}

TY - JOUR

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

AU - Volikos, E

AU - J, Robinson

AU - K, Aittomaki

AU - JP, Mecklin

AU - H, Jarvinen

AU - AM, Westerman

AU - FW, de Rooji

AU - T, Vogel

AU - G, Moeslein

AU - V, Launonen

AU - Tomlinson, Ian

AU - AR, Silver

AU - LA, Aaltonen

PY - 2006

Y1 - 2006

U2 - 10.1136/jmg.2005.039875

DO - 10.1136/jmg.2005.039875

M3 - Article

SN - 0022-2593

VL - 43

SP - e18-e18

JO - Journal of Medical Genetics

JF - Journal of Medical Genetics

IS - 5

ER -