Search Results - Twelkemeyer, S

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    Mutation analysis in hereditary haemorrhagic telangiectasia in Germany reveals 11 novel ENG and 12 novel ACVRL1/ALK1 mutations

    Mutation analysis in hereditary haemorrhagic telangiectasia in Germany reveals 11 novel ENG and 12 novel ACVRL1/ALK1 mutations by Wehner, L-E, Folz, BJ, Argyriou, L, Twelkemeyer, S, Teske, U, Geisthoff, UW, Werner, JA, Engel, W, Nayernia, K

    Published in Clinical genetics
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  2. 2
    Novel mutations in the ENG and ACVRL1 genes causing hereditary hemorrhagic teleangiectasia

    Novel mutations in the ENG and ACVRL1 genes causing hereditary hemorrhagic teleangiectasia by Argyriou, Loukas, Twelkemeyer, Stefan, Panchulidze, Irakli, Wehner, Lars-Erik, Teske, Ute, Engel, Wolfgang, Nayernia, Karim

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    Short Report: Mutation analysis in hereditary haemorrhagic telangiectasia in Germany reveals 11 novel ENG and 12 novel ACVRL1/ALK1 mutations

    Short Report: Mutation analysis in hereditary haemorrhagic telangiectasia in Germany reveals 11 novel ENG and 12 novel ACVRL1/ALK1 mutations by L-E Wehner, Folz, B J, Argyriou, L, Twelkemeyer, S, Teske, U, Geisthoff, U W, Werner, JA, Engel, W, Nayernia, K

    Published in Clinical genetics
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