A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States

HT Lynch; SM Coronel; R Okimoto; H Hampel; K Sweet; JF Lynch; A Barrows; J (Juul) van Wijnen; H van der Klift; Patrick Franken; Anja Wagner; Riccardo Fodde; A de la Chapelle

doi:10.1001/jama.291.6.718

A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States

HT Lynch, SM Coronel, R Okimoto, H Hampel, K Sweet, JF Lynch, A Barrows, J (Juul) van Wijnen, H van der Klift, Patrick Franken, Anja Wagner, Riccardo Fodde, A de la Chapelle

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

79 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	2473-2481
Number of pages	9
Journal	Clinical Cancer Research
Volume	10
DOIs	https://doi.org/10.1001/jama.291.6.718
Publication status	Published - 2004

Research programs

EMC MGC-02-96-01

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

Access to Document

10.1001/jama.291.6.718

http://hdl.handle.net/1765/56712

Cite this

Lynch, HT., Coronel, SM., Okimoto, R., Hampel, H., Sweet, K., Lynch, JF., Barrows, A., van Wijnen, J., van der Klift, H., Franken, P., Wagner, A., Fodde, R., & de la Chapelle, A. (2004). A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States. Clinical Cancer Research, 10, 2473-2481. https://doi.org/10.1001/jama.291.6.718

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AU - Hampel, H

AU - Sweet, K

AU - Lynch, JF

AU - Barrows, A

AU - van Wijnen, J (Juul)

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AU - Fodde, Riccardo

AU - de la Chapelle, A

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JO - Clinical Cancer Research

JF - Clinical Cancer Research

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