检索结果 - M.W. Wessels

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  1. 1
    Further delineation of Pitt-Hopkins syndrome: phenotypic and genotypic description of 16 novel patients

    Further delineation of Pitt-Hopkins syndrome: phenotypic and genotypic description of 16 novel patients 由 Christiane Zweier, Heinrich Sticht, Emilia K. Bijlsma, Jill Clayton‐Smith, Susanne E. Boonen, Alan Fryer, Marie T. Greally, Ling Hoffmann, Nicolette S. den Hollander, Marjolijn C.J. Jongmans, Sarina G. Kant, Matthew King, Sally Ann Lynch, Shane McKee, Alina T. Midro, Park Sm, Valeria Ricotti, E Tarantino, M.W. Wessels, Maarit Peippo, Anita Rauch

    出版 2008
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    Novel Mutations Including Deletions of the Entire<i>OFD1</i>Gene in 30 Families with Type 1 Orofaciodigital Syndrome: A Study of the Extensive Clinical Variability

    Novel Mutations Including Deletions of the Entire<i>OFD1</i>Gene in 30 Families with Type 1 Orofaciodigital Syndrome: A Study of the Extensive Clinical Variability 由 Izak Johannes Bisschoff, Christine Zeschnigk, Denise Horn, Brigitte Wellek, Angelika Rieß, M.W. Wessels, P J Willems, Peter Bjødstrup Jensen, Andreas Busche, Jens Bekkebraten, Maya Chopra, Hanne Hove, Christina Evers, Ketil Heimdal, Ann-Sophie Kaiser, Erdmut Kunstmann, Kristina Lagerstedt‐Robinson, Maja Linné, Patricia Martín, James McGrath, Winnie Pradel, Katrina Prescott, Bernd Roesler, Goražd Rudolf, Ulrike Siebers‐Renelt, Nataliya Tyshchenko, Dagmar Wieczorek, G. Wolff, William B. Dobyns, Deborah Morris‐Rosendahl

    出版 2012
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