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Page 1
Phenotypic variability associated with WNT10A nonsense mutations.
Van Geel M, Gattas M, Kesler Y, Tong P, Yan H, Tran K, Steijlen PM, Murrell DF, Van Steensel MA. Van Geel M, et al. Among authors: van steensel ma. Br J Dermatol. 2010 Jun;162(6):1403-6. doi: 10.1111/j.1365-2133.2010.09703.x. Epub 2010 Feb 15. Br J Dermatol. 2010. PMID: 20163410 No abstract available.
A new type of erythrokeratoderma.
van Steensel MA, van Geel M, Steijlen PM. van Steensel MA, et al. Among authors: van geel m. Br J Dermatol. 2005 Jan;152(1):155-8. doi: 10.1111/j.1365-2133.2005.06319.x. Br J Dermatol. 2005. PMID: 15656818
Novel EBP gene mutations in Conradi-Hünermann-Happle syndrome.
Steijlen PM, van Geel M, Vreeburg M, Marcus-Soekarman D, Spaapen LJ, Castelijns FC, Willemsen M, van Steensel MA. Steijlen PM, et al. Among authors: van steensel ma, van geel m. Br J Dermatol. 2007 Dec;157(6):1225-9. doi: 10.1111/j.1365-2133.2007.08254.x. Epub 2007 Oct 18. Br J Dermatol. 2007. PMID: 17949453
Chanarin-Dorfman syndrome caused by a novel splice site mutation in ABHD5.
Badeloe S, van Geel M, Nagtzaam I, Rubio-Gozalbo ME, Oei RL, Steijlen PM, van Steensel MA. Badeloe S, et al. Among authors: van steensel ma, van geel m. Br J Dermatol. 2008 Jun;158(6):1378-80. doi: 10.1111/j.1365-2133.2008.08544.x. Epub 2008 Apr 10. Br J Dermatol. 2008. PMID: 18410411 No abstract available.
217 results