Home > Publications database > Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence > print

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024 7 _ |a 10.1186/s12920-023-01469-z
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100 1 _ |a Hassanin, Emadeldin
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245 _ _ |a Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence
260 _ _ |a London
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700 1 _ |a Spier, Isabel
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700 1 _ |a Bobbili, Dheeraj R.
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700 1 _ |a Aldisi, Rana
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700 1 _ |a Klinkhammer, Hannah
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700 1 _ |a David, Friederike
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700 1 _ |a Dueñas, Nuria
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700 1 _ |a Hüneburg, Robert
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700 1 _ |a Perne, Claudia
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700 1 _ |a Brunet, Joan
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700 1 _ |a Capella, Gabriel
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700 1 _ |a Nöthen, Markus M.
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700 1 _ |a Forstner, Andreas J.
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700 1 _ |a Mayr, Andreas
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700 1 _ |a Krawitz, Peter
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700 1 _ |a May, Patrick
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700 1 _ |a Aretz, Stefan
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700 1 _ |a Maj, Carlo
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773 _ _ |a 10.1186/s12920-023-01469-z
|g Vol. 16, no. 1, p. 42
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