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Page 1
Rapid antibody test for fragile X syndrome.
Willemsen R, Mohkamsing S, de Vries B, Devys D, van den Ouweland A, Mandel JL, Galjaard H, Oostra B. Willemsen R, et al. Among authors: van den ouweland a. Lancet. 1995 May 6;345(8958):1147-8. doi: 10.1016/s0140-6736(95)90979-6. Lancet. 1995. PMID: 7723547
Rapid antibody test for diagnosing fragile X syndrome: a validation of the technique.
Willemsen R, Smits A, Mohkamsing S, van Beerendonk H, de Haan A, de Vries B, van den Ouweland A, Sistermans E, Galjaard H, Oostra BA. Willemsen R, et al. Among authors: van beerendonk h, van den ouweland a. Hum Genet. 1997 Mar;99(3):308-11. doi: 10.1007/s004390050363. Hum Genet. 1997. PMID: 9050914 Free article.
Interaction between hamartin and tuberin, the TSC1 and TSC2 gene products.
van Slegtenhorst M, Nellist M, Nagelkerken B, Cheadle J, Snell R, van den Ouweland A, Reuser A, Sampson J, Halley D, van der Sluijs P. van Slegtenhorst M, et al. Among authors: van der sluijs p, van den ouweland a. Hum Mol Genet. 1998 Jun;7(6):1053-7. doi: 10.1093/hmg/7.6.1053. Hum Mol Genet. 1998. PMID: 9580671 Free article.
Large deletion at the TSC1 locus in a family with tuberous sclerosis complex.
Nellist M, Sancak O, Goedbloed MA, van Veghel-Plandsoen M, Maat-Kievit A, Lindhout D, Eussen BH, de Klein A, Halley DJ, van den Ouweland AM. Nellist M, et al. Among authors: van veghel plandsoen m, van den ouweland am. Genet Test. 2005 Fall;9(3):226-30. doi: 10.1089/gte.2005.9.226. Genet Test. 2005. PMID: 16225402
Somatic mosaicism and clinical variation in tuberous sclerosis complex.
Verhoef S, Vrtel R, van Essen T, Bakker L, Sikkens E, Halley D, Lindhout D, van den Ouweland A. Verhoef S, et al. Among authors: van essen t, van den ouweland a. Lancet. 1995 Jan 21;345(8943):202. doi: 10.1016/s0140-6736(95)90213-9. Lancet. 1995. PMID: 7823706 No abstract available.
Common C-to-T substitution at position -480 of the hepatic lipase promoter associated with a lowered lipase activity in coronary artery disease patients.
Jansen H, Verhoeven AJ, Weeks L, Kastelein JJ, Halley DJ, van den Ouweland A, Jukema JW, Seidell JC, Birkenhäger JC. Jansen H, et al. Among authors: van den ouweland a. Arterioscler Thromb Vasc Biol. 1997 Nov;17(11):2837-42. doi: 10.1161/01.atv.17.11.2837. Arterioscler Thromb Vasc Biol. 1997. PMID: 9409263
Functional characterization of the TSC2 c.3598C>T (p.R1200W) missense mutation that co-segregates with tuberous sclerosis complex in mildly affected kindreds.
Wentink M, Nellist M, Hoogeveen-Westerveld M, Zonnenberg B, van der Kolk D, van Essen T, Park SM, Woods G, Cohn-Hokke P, Brussel W, Smeets E, Brooks A, Halley D, van den Ouweland A, Maat-Kievit A. Wentink M, et al. Among authors: van essen t, van den ouweland a, van der kolk d. Clin Genet. 2012 May;81(5):453-61. doi: 10.1111/j.1399-0004.2011.01648.x. Epub 2011 Mar 10. Clin Genet. 2012. PMID: 21332470
300 results