Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome)

Y.M. Hendriks; S Jagmohan-Changur; HM van der Klift; H. Morreau; M. van Puijenbroek; C. Tops; T. van Os; A Wagner; M.G.E.M. Ausems; X et al.

Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome)

Translated title of the contribution: Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome)

Y.M. Hendriks, S Jagmohan-Changur, HM van der Klift, H. Morreau, M. van Puijenbroek, C. Tops, T. van Os, A Wagner, M.G.E.M. Ausems, X et al.

Department of Genetics

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

Translated title of the contribution	Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome)
Original language	Undefined/Unknown
Pages (from-to)	312-322
Number of pages	11
Journal	Gastroenterology
Volume	130
Issue number	2
Publication status	Published - 2006

Cite this

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title = "Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome)",

author = "Y.M. Hendriks and S Jagmohan-Changur and {van der Klift}, HM and H. Morreau and {van Puijenbroek}, M. and C. Tops and {van Os}, T. and A Wagner and M.G.E.M. Ausems and {et al.}, X",

year = "2006",

language = "Undefined/Unknown",

volume = "130",

pages = "312--322",

journal = "Gastroenterology",

issn = "0016-5085",

publisher = "W.B. Saunders",

number = "2",

}

TY - JOUR

T1 - Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome)

AU - Hendriks, Y.M.

AU - Jagmohan-Changur, S

AU - van der Klift, HM

AU - Morreau, H.

AU - van Puijenbroek, M.

AU - Tops, C.

AU - van Os, T.

AU - Wagner, A

AU - Ausems, M.G.E.M.

AU - et al., X

PY - 2006

Y1 - 2006

M3 - Article

SN - 0016-5085

VL - 130

SP - 312

EP - 322

JO - Gastroenterology

JF - Gastroenterology

IS - 2

ER -