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Molecular and clinico-pathological features of two families with the HNPCC syndrome and unusual phenotypes

Publication status:: Published

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APA Style

Tomlinson, I., Beck, N., Homfray, T., Harocopos, C., Adams, M., Hodgson, S., Markie, D., & Bodmer, W. (1997). Molecular and clinico-pathological features of two families with the HNPCC syndrome and unusual phenotypes. GI CANCER, 2(2), 89–98.

MLA Style

Tomlinson, I., et al. “Molecular and Clinico-Pathological Features of Two Families with the HNPCC Syndrome and Unusual Phenotypes.” GI CANCER, vol. 2, no. 2, 1997, pp. 89–98.

Chicago Style

Tomlinson, I, N Beck, T Homfray, C Harocopos, M Adams, S Hodgson, D Markie, and W Bodmer. 1997. “Molecular and Clinico-Pathological Features of Two Families with the HNPCC Syndrome and Unusual Phenotypes.” GI CANCER 2 (2): 89–98.
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+ Tomlinson, I More by this author

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+ Beck, N More by this author

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+ Homfray, T More by this author

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+ Harocopos, C More by this author

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+ Adams, M More by this author

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Journal:: GI CANCER More from this journal
Volume:: 2
Issue:: 2
Pages:: 89-98
Publication date:: 1997-01-01
ISSN:: 1064-9700

Keywords:: Muir-Torre

GI adenomas

juvenile polyposis

HNPCC
Pubs id:: pubs:487609
UUID:: uuid:5216f06b-3bba-4b05-ba44-4f3bc3228155
Local pid:: pubs:487609
Source identifiers:: 487609
Deposit date:: 2014-10-29

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Copyright date:: 1997

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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