Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene

Anja Wagner; A Barrows; JT Wijnen; H van der Klift; PF Franken; P Verkuijlen; H Nakagawa; M Geugien; S Jaghmohan-Changur; C Breukel; EJ Meijers-Heijboer; H Morreau; M van Puijenbroek; J Burn; S Coronel; Y Kinarsky; R Okimoto; P Watson; JF Lynch; A de la Chapelle; HT Lynch; Riccardo Fodde

doi:10.1086/373963

Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene

Anja Wagner, A Barrows, JT Wijnen, H van der Klift, PF Franken, P Verkuijlen, H Nakagawa, M Geugien, S Jaghmohan-Changur, C Breukel, EJ Meijers-Heijboer, H Morreau, M van Puijenbroek, J Burn, S Coronel, Y Kinarsky, R Okimoto, P Watson, JF Lynch, A de la ChapelleHT Lynch, Riccardo Fodde

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

182 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	1088-1099
Number of pages	12
Journal	American Journal of Human Genetics
Volume	72
Issue number	5
DOIs	https://doi.org/10.1086/373963
Publication status	Published - 2003

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EMC MGC-02-96-01

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10.1086/373963

http://hdl.handle.net/1765/56855

Cite this

Wagner, A., Barrows, A., Wijnen, JT., van der Klift, H., Franken, PF., Verkuijlen, P., Nakagawa, H., Geugien, M., Jaghmohan-Changur, S., Breukel, C., Meijers-Heijboer, EJ., Morreau, H., van Puijenbroek, M., Burn, J., Coronel, S., Kinarsky, Y., Okimoto, R., Watson, P., Lynch, JF., ... Fodde, R. (2003). Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene. American Journal of Human Genetics, 72(5), 1088-1099. https://doi.org/10.1086/373963

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title = "Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene",

author = "Anja Wagner and A Barrows and JT Wijnen and {van der Klift}, H and PF Franken and P Verkuijlen and H Nakagawa and M Geugien and S Jaghmohan-Changur and C Breukel and EJ Meijers-Heijboer and H Morreau and {van Puijenbroek}, M and J Burn and S Coronel and Y Kinarsky and R Okimoto and P Watson and JF Lynch and {de la Chapelle}, A and HT Lynch and Riccardo Fodde",

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doi = "10.1086/373963",

language = "Undefined/Unknown",

volume = "72",

pages = "1088--1099",

journal = "American Journal of Human Genetics",

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Wagner, A, Barrows, A, Wijnen, JT, van der Klift, H, Franken, PF, Verkuijlen, P, Nakagawa, H, Geugien, M, Jaghmohan-Changur, S, Breukel, C, Meijers-Heijboer, EJ, Morreau, H, van Puijenbroek, M, Burn, J, Coronel, S, Kinarsky, Y, Okimoto, R, Watson, P, Lynch, JF, de la Chapelle, A, Lynch, HT & Fodde, R 2003, 'Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene', American Journal of Human Genetics, vol. 72, no. 5, pp. 1088-1099. https://doi.org/10.1086/373963

Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene. / Wagner, Anja; Barrows, A; Wijnen, JT et al.
In: American Journal of Human Genetics, Vol. 72, No. 5, 2003, p. 1088-1099.

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

TY - JOUR

T1 - Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene

AU - Wagner, Anja

AU - Barrows, A

AU - Wijnen, JT

AU - van der Klift, H

AU - Franken, PF

AU - Verkuijlen, P

AU - Nakagawa, H

AU - Geugien, M

AU - Jaghmohan-Changur, S

AU - Breukel, C

AU - Meijers-Heijboer, EJ

AU - Morreau, H

AU - van Puijenbroek, M

AU - Burn, J

AU - Coronel, S

AU - Kinarsky, Y

AU - Okimoto, R

AU - Watson, P

AU - Lynch, JF

AU - de la Chapelle, A

AU - Lynch, HT

AU - Fodde, Riccardo

PY - 2003

Y1 - 2003

U2 - 10.1086/373963

DO - 10.1086/373963

M3 - Article

SN - 0002-9297

VL - 72

SP - 1088

EP - 1099

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

IS - 5

ER -

Wagner A, Barrows A, Wijnen JT, van der Klift H, Franken PF, Verkuijlen P et al. Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene. American Journal of Human Genetics. 2003;72(5):1088-1099. doi: 10.1086/373963