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dr. T.G.W. (Tom) Letteboer

dr. T.G.W. (Tom) Letteboer

Assistant Professor - medical

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Research Output (54)

Hereditary hemorrhagic telangiectasia: How accurate are the clinical criteria?

van Gent M.W.F., Velthuis S., Post M.C., Snijder R.J., Westermann C.J.J., Letteboer T.G.W., Mager J.J. 2013, In: American Journal of Medical Genetics. Part A. 161 , p. 461-466 6 p.

Adherence to microsatellite instability testin in young-onset colorectal cancer patients.

Kessels K., Fidder H.H., de Groot N.L., Letteboer T.G.W., Timmer R., van Dalen T., Consten E.C., Offerhaus G.J.A., Siersema P.D. 2013, In: Diseases of the Colon & Rectum. 56 , p. 825-833 9 p.

Erfelijke darmkanker: Is het bevolkingsonderzoek toereikend?

Letteboer T.G.W. 2013, In: MAGMA. 19 , p. 7-7 1 p.

Risks of less common cancers in proven mutation carriers with lynch syndrome

Engel C., Loeffler M., Steinke V., Rahner N., Holinski-Feder E., Dietmaier W., Schackert H.K., Goergens H., von Knebel Doeberitz M., Goecke T.O., Schmiegel W., Buettner R., Moeslein G., Letteboer T.G.W., Gómez García E., Hes F., Hoogerbrugge N., Menko F.H., van Os Th.A.M., Sijmons R.H., Wagner A, Kluijt I., Propping P., Vasen H.F.A. 2012, In: Journal of Clinical Oncology. 10 , p. 4409-4415 7 p.

Erratum: Mouse and human strategies identify PTPN14 as a modifier of angiogenesis and hereditary haemorrhagic telangiectasia

Benzinou M., Clermont F.F., Letteboer T.G.W., Kim J., Espejel S., Harradine K.A., Arbelaez J., Luu M.T., Roy R., Quigley D., Nakayama Higgens M., Zaid M., Aouizerat B.E., Ploos van Amstel J.K., Giraud S., Dupuis-Girod S., Lesca G., Plauchu H., Hughes C.C.W., Westermann C.J.J., Akhurst R.J. 2012, In: Nature Communications [E]. 3 , p. 1148 1 p.

Mouse and human strategies identify PTPN14 as a modifier of angiogenesis and hereditary haemorrhagic telangiectasia

Benzinou M., Clermont F.F., Letteboer T., Kim J.-H., Espejel S., Harradine K.A., Arbelaez J., Luu M.T., Roy R., Quigley D., Higgins N.K., Zaid M., Aouizerat B.E., Ploos van Amstel J.K., Giraud S., Dupuis-Girod Sophie, Lesca G., Plauchu H., Hughes C.C.W., Westermann C.J.J., Akhurst R.J. 2012, In: Nature Communications [E]. 3 , p. 616 1 p.

Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germline

Kloosterman W.P., van Binsbergen E., Poot M., Duran K.J., Hochstenbach R., van Roosmalen M., Guryev V., de Bruijn M.E., Renkens I.J., van Nesselrooij B.P.M., Letteboer T.G.W., Bakker S.C., Cuppen E.P.J.G. 28 May 2011,

Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germline

Kloosterman W.P., Guryev V., van Roosmalen M.J., Duran K.J., de Bruijn E., Bakker S.C.M., Letteboer T.G.W., van Nesselrooij B.P.M., Hochstenbach P.F.R., Poot M., Cuppen E.P.J.G. 2011, In: Human Molecular Genetics. 20 , p. 1916-1924 9 p.

Is hereditary haemorrhagic telangiectasia rare in the black race? The first sub-Saharan mutation

Westermann C.J., Kitonyi G.W., Letteboer T.G.W. 2011, In: Haemophilia. 17 , p. e244-e244 1 p.

Hereditary hemorrhagic telangiectasia clinical and molecular genetics

Letteboer T.G.W. 10 Nov 2010, 170 p.

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