MSH2 genomic deletions are a frequent cause of HNPCC [2]

J. Wijnen; H. Van der Klift; H. F.A. Vasen; P. M. Khan; F. Menko; C. Tops; H. M. Heijboer; D. Lindhout; P. Moller; R. Fodde

doi:10.1038/3795

MSH2 genomic deletions are a frequent cause of HNPCC [2]

J. Wijnen, H. Van der Klift, H. F.A. Vasen, P. M. Khan, F. Menko, C. Tops, H. M. Heijboer, D. Lindhout, P. Moller, R. Fodde^*

^*Corresponding author for this work

Research output: Contribution to journal › Letter › Academic › peer-review

Original language	English
Pages (from-to)	326-328
Number of pages	3
Journal	Nature Genetics
Volume	20
Issue number	4
DOIs	https://doi.org/10.1038/3795
Publication status	Published - 1998
Externally published	Yes

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10.1038/3795

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@article{b1e77ea74bcb40058ee01dfc0377004e,

title = "MSH2 genomic deletions are a frequent cause of HNPCC [2]",

author = "J. Wijnen and \{Van der Klift\}, H. and Vasen, \{H. F.A.\} and Khan, \{P. M.\} and F. Menko and C. Tops and Heijboer, \{H. M.\} and D. Lindhout and P. Moller and R. Fodde",

year = "1998",

doi = "10.1038/3795",

language = "English",

volume = "20",

pages = "326--328",

journal = "Nature Genetics",

issn = "1061-4036",

publisher = "Nature Research",

number = "4",

}

TY - JOUR

T1 - MSH2 genomic deletions are a frequent cause of HNPCC [2]

AU - Wijnen, J.

AU - Van der Klift, H.

AU - Vasen, H. F.A.

AU - Khan, P. M.

AU - Menko, F.

AU - Tops, C.

AU - Heijboer, H. M.

AU - Lindhout, D.

AU - Moller, P.

AU - Fodde, R.

PY - 1998

Y1 - 1998

UR - https://www.scopus.com/pages/publications/0031795020

U2 - 10.1038/3795

DO - 10.1038/3795

M3 - Letter

C2 - 9843200

AN - SCOPUS:0031795020

SN - 1061-4036

VL - 20

SP - 326

EP - 328

JO - Nature Genetics

JF - Nature Genetics

IS - 4

ER -

MSH2 genomic deletions are a frequent cause of HNPCC [2]

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