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Items: 9

1.

The clinical consequences of hemizygosity across 2 MB of 10q23 are restricted to Cowden syndrome.

Lewis CM, Bu D, Sarode V, Robinson L, Wilson KS, Viscusi RK, Eng C, Euhus DM.

Breast Cancer Res Treat. 2012 Dec;136(3):911-8. doi: 10.1007/s10549-012-2322-z. Epub 2012 Nov 7.

PMID:
23132533
2.

The role of PTEN, a phosphatase gene, in inherited and sporadic nonmedullary thyroid tumors.

Eng C.

Recent Prog Horm Res. 1999;54:441-52; discussion 453. Review.

PMID:
10548886
3.

[Cowden disease].

Sawada T, Hamano N, Suzuki A, Okada T, Mabuchi H.

Nihon Rinsho. 2000 Jul;58(7):1479-83. Review. Japanese.

PMID:
10921327
4.

PTEN hamartoma tumor syndrome: clinical risk assessment and management protocol.

Ngeow J, Eng C.

Methods. 2015 May;77-78:11-9. doi: 10.1016/j.ymeth.2014.10.011. Epub 2014 Oct 22. Review.

PMID:
25461771
5.

Cowden syndrome and the PTEN hamartoma tumor syndrome: systematic review and revised diagnostic criteria.

Pilarski R, Burt R, Kohlman W, Pho L, Shannon KM, Swisher E.

J Natl Cancer Inst. 2013 Nov 6;105(21):1607-16. doi: 10.1093/jnci/djt277. Epub 2013 Oct 17. Review.

PMID:
24136893
6.

Cowden syndrome (multiple hamartoma syndrome).

Mallory SB.

Dermatol Clin. 1995 Jan;13(1):27-31. Review.

PMID:
7712647
7.

Genetics of Cowden syndrome: through the looking glass of oncology.

Eng C.

Int J Oncol. 1998 Mar;12(3):701-10. Review.

PMID:
9472113
8.
9.

Juvenile polyposis and other intestinal polyposis syndromes with microdeletions of chromosome 10q22-23.

Dahdaleh FS, Carr JC, Calva D, Howe JR.

Clin Genet. 2012 Feb;81(2):110-6. doi: 10.1111/j.1399-0004.2011.01763.x. Epub 2011 Sep 6. Review.

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