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Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis.
Smit DL, Mensenkamp AR, Badeloe S, Breuning MH, Simon ME, van Spaendonck KY, Aalfs CM, Post JG, Shanley S, Krapels IP, Hoefsloot LH, van Moorselaar RJ, Starink TM, Bayley JP, Frank J, van Steensel MA, Menko FH. Smit DL, et al. Among authors: starink tm. Clin Genet. 2011 Jan;79(1):49-59. doi: 10.1111/j.1399-0004.2010.01486.x. Clin Genet. 2011. PMID: 20618355
Localization of the gene for Cowden disease to chromosome 10q22-23.
Nelen MR, Padberg GW, Peeters EA, Lin AY, van den Helm B, Frants RR, Coulon V, Goldstein AM, van Reen MM, Easton DF, Eeles RA, Hodgsen S, Mulvihill JJ, Murday VA, Tucker MA, Mariman EC, Starink TM, Ponder BA, Ropers HH, Kremer H, Longy M, Eng C. Nelen MR, et al. Among authors: starink tm. Nat Genet. 1996 May;13(1):114-6. doi: 10.1038/ng0596-114. Nat Genet. 1996. PMID: 8673088
[Patient with Cowden syndrome].
Stouthamer A, Menke HE, Starink TM. Stouthamer A, et al. Among authors: starink tm. Ned Tijdschr Geneeskd. 1999 Sep 25;143(39):1980-1. Ned Tijdschr Geneeskd. 1999. PMID: 10610484 Dutch. No abstract available.
Decreased natural killer cell activity in Cowden's syndrome.
Starink TM, van der Veen JP, Goldschmeding R. Starink TM, et al. J Am Acad Dermatol. 1986 Aug;15(2 Pt 1):294-6. doi: 10.1016/s0190-9622(86)80258-4. J Am Acad Dermatol. 1986. PMID: 3745534 No abstract available.
84 results