Clinical and Mutational Spectrum of Mowat–Wilson Syndrome
Christiane Zweier(Friedrich-Alexander-Universität Erlangen-Nürnberg), Christian T. Thiel(Friedrich-Alexander-Universität Erlangen-Nürnberg), Andreas Dufke(University of Tübingen), Yanick J. Crow(St James's University Hospital), Peter Meinecke(Kinderkrebs-Zentrum Hamburg), Mohnish Suri(Nottingham City Hospital), Sirpa Ala‐Mello(Helsinki University Hospital), Frits A. Beemer(University Medical Center Utrecht), Sergio Bernasconi(University of Parma), Paolo Pietro Bianchi(University of Bergamo), Andrea Bier, Koenraad Devriendt, Boyan Dimitrov, Helen V. Firth(Addenbrooke's Hospital), Renata C. Gallagher(Pediatrics and Genetics), Livia Garavelli(Azienda Sanitaria Unità Locale di Reggio Emilia), Gabriele Gillessen‐Kaesbach(Essen University Hospital), Louanne Hudgins(Pediatrics and Genetics), Helena Kääriäinen(University of Turku), Susan Karstens, Ian D. Krantz(Children's Hospital of Philadelphia), Anca Mannhardt(Werner Otto Stiftung), Līvija Medne(Children's Hospital of Philadelphia), Jürgen Mücke(Medical Genetics Center), Maria Kibæk(Odense University Hospital), Lotte Krogh(Odense University Hospital), Maarit Peippo(Väestöliitto), Olaf Rittinger(Unfallkrankenhaus Salzburg), Solveig Schulz(University Hospital Magdeburg), Susan Schelley(Pediatrics and Genetics), I. Karen Temple, N R Dennis, Marjo S. van der Knaap(Amsterdam UMC Location Vrije Universiteit Amsterdam), Patricia G. Wheeler(Nemours Children's Clinic), Baruch Yerushalmi(Soroka Medical Center), Martin Zenker(Friedrich-Alexander-Universität Erlangen-Nürnberg), Heide Seidel(Ludwig-Maximilians-Universität München), A.M.A. Lachmeijer(Amsterdam UMC Location Vrije Universiteit Amsterdam), Trine Prescott, Cornelia Kraus(Friedrich-Alexander-Universität Erlangen-Nürnberg), R. Brian Lowry(Alberta Children's Hospital), Anita Rauch(Friedrich-Alexander-Universität Erlangen-Nürnberg)
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