4 results for author:"van der Vlies P." in Literature citations
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| Exempting homologous pseudogene sequences from polymerase chain reaction amplification allows genomic keratin 14 hotspot analysis. Hut P.H.L., van der Vlies P., Jonkman M.F., Verlind E., Shimizu H., Buys C.H.C.M., Scheffer H. J. Invest. Dermatol. 114:616-619(2000) · UniProtKB (1) |
| Epidermolysis bullosa simplex with mottled pigmentation: clinical aspects and confirmation of the P24L mutation in the KRT5 gene in further patients. Moog U., de Die-Smulders C.E.M., Scheffer H., van der Vlies P., Henquet C.J.M., Jonkman M.F. Am. J. Med. Genet. 86:376-379(1999) · UniProtKB (1) |
| Three novel KCNA1 mutations in episodic ataxia type I families. Scheffer H., Brunt E.R.P., Mol G.J.J., van der Vlies P., Stulp R.P., Verlind E., Mantel G., Averyanov Y.N., Hofstra R.M.W., Buys C.H.C.M. Hum. Genet. 102:464-466(1998) · UniProtKB (1) |
| Mutational scanning of large genes by extensive PCR multiplexing and two-dimensional electrophoresis: application to the RB1 gene. Van Orsouw N.J., Li D., van der Vlies P., Scheffer H., Eng C., Buys C.H.C.M., Li F.P., Vijg J. Hum. Mol. Genet. 5:755-761(1996) · UniProtKB (1) |