MSH2 genomic deletions are a frequent cause of HNPCC

J. Wijnen; H. van der Klift; H. Vasen; P. M. Khan; F. Menko; C. Tops; H. Meijers Heijboer; D. Lindhout; P. Møller; R. Fodde

doi:https://doi.org/10.1038/3795

MSH2 genomic deletions are a frequent cause of HNPCC

J. Wijnen, H. van der Klift, H. Vasen, P. M. Khan, F. Menko, C. Tops, H. Meijers Heijboer, D. Lindhout, P. Møller, R. Fodde

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Research output: Contribution to journal › Comment/Letter to the editor › Academic

197 Citations (Scopus)

Original language	English
Pages (from-to)	326-328
Journal	Nature Genetics
Volume	20
Issue number	4
DOIs	https://doi.org/10.1038/3795
Publication status	Published - 1998

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https://doi.org/10.1038/3795

Cite this

@article{8b5bf561f21843c8a974f47dcef5f12c,

title = "MSH2 genomic deletions are a frequent cause of HNPCC",

author = "J. Wijnen and {van der Klift}, H. and H. Vasen and Khan, {P. M.} and F. Menko and C. Tops and {Meijers Heijboer}, H. and D. Lindhout and P. M{\o}ller and R. Fodde",

year = "1998",

doi = "https://doi.org/10.1038/3795",

language = "English",

volume = "20",

pages = "326--328",

journal = "Nature Genetics",

issn = "1061-4036",

publisher = "Nature Publishing Group",

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TY - JOUR

T1 - MSH2 genomic deletions are a frequent cause of HNPCC

AU - Wijnen, J.

AU - van der Klift, H.

AU - Vasen, H.

AU - Khan, P. M.

AU - Menko, F.

AU - Tops, C.

AU - Meijers Heijboer, H.

AU - Lindhout, D.

AU - Møller, P.

AU - Fodde, R.

PY - 1998

Y1 - 1998

U2 - https://doi.org/10.1038/3795

DO - https://doi.org/10.1038/3795

M3 - Comment/Letter to the editor

C2 - 9843200

SN - 1061-4036

VL - 20

SP - 326

EP - 328

JO - Nature Genetics

JF - Nature Genetics

IS - 4

ER -