Search Results - Wouters, Vinciane

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  1. 1
    Hereditary cutaneomucosal venous malformations are caused by TIE2 mutations with widely variable hyper-phosphorylating effects

    Hereditary cutaneomucosal venous malformations are caused by TIE2 mutations with widely variable hyper-phosphorylating effects by Wouters, Vinciane, Limaye, Nisha, Uebelhoer, Melanie, Irrthum, Alexandre, Boon, Laurence M, Mulliken, John B, Enjolras, Odile, Baselga, Eulalia, Berg, Jonathan, Dompmartin, Anne, Ivarsson, Sten A, Kangesu, Loshan, Lacassie, Yves, Murphy, Jill, Teebi, Ahmad S, Penington, Anthony, Rieu, Paul, Vikkula, Miikka

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  2. 2
    PTHR1 mutations associated with Ollier disease result in receptor loss of function

    PTHR1 mutations associated with Ollier disease result in receptor loss of function by Couvineau, Alain, Wouters, Vinciane, Bertrand, Guylène, Rouyer, Christiane, Gérard, Bénédicte, Boon, Laurence M., Grandchamp, Bernard, Vikkula, Miikka, Silve, Caroline

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  3. 3
    Common Somatic Alterations Identified in Maffucci Syndrome by Molecular Karyotyping

    Common Somatic Alterations Identified in Maffucci Syndrome by Molecular Karyotyping by Amyere, Mustapha, Dompmartin, Anne, Wouters, Vinciane, Enjolras, Odile, Kaitila, Ilkka, Docquier, Pierre-Louis, Godfraind, Catherine, Mulliken, John Butler, Boon, Laurence Myriam, Vikkula, Miikka

    Published in Molecular syndromology
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  4. 4
    Hereditary cutaneomucosal venous malformations are caused by TIE2 mutations with widely variable hyper-phosphorylati ng effects

    Hereditary cutaneomucosal venous malformations are caused by TIE2 mutations with widely variable hyper-phosphorylati ng effects by WOUTERS, Vinciane, LIMAYE, Nisha, IVARSSON, Sten A, KANGESU, Loshan, LACASSIE, Yves, MURPHY, Jill, TEEBI, Ahmad S, PENINGTON, Anthony, RIEU, Paul, VIKKULA, Miikka, UEBELHOER, Melanie, IRRTHUM, Alexandre, BOON, Laurence M, MULLIKEN, John B, ENJOLRAS, Odile, BASELGA, Eulalia, BERG, Jonathan, DOMPMARTIN, Anne

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