Mutations in the Pericentrin ( <i>PCNT</i> ) Gene Cause Primordial Dwarfism
Anita Rauch(University of Zurich), André Reis(Charité - Universitätsmedizin Berlin), Christiane Zweier(Friedrich-Alexander-Universität Erlangen-Nürnberg), Yanick J. Crow(Délégation Paris 5), André Mégarbané(University Medical Center Groningen), Han G. Brunner(Radboud University Nijmegen), Kristin Becker(Glan Clwyd Hospital), Richard C. Trembath(University Medical Center Groningen), Lihadh Al‐Gazali(United Arab Emirates University), Arif B. Ekici(University Medical Center Groningen), Stephanie Spranger(University Medical Center Groningen), Raoul C. M. Hennekam(Emma Kinderziekenhuis), Anthonie J. van Essen(University Medical Center Groningen), Timm O. Goecke(University Medical Center Groningen), Annick Toutain(University Medical Center Groningen), Krystyńa Chrzańowska(University Medical Center Groningen), Peter Meinecke(University Medical Center Groningen), Francis de Zegher(University Medical Center Groningen), Egbert Voß(University Medical Center Groningen), Christian T. Thiel(University Medical Center Groningen), Koenraad Devriendt(University Medical Center Groningen), Esther Kinning(University Medical Center Groningen), Ursula Wick(University Medical Center Groningen), Robert K. Semple(University of Cambridge), Louise C. Wilson(University Medical Center Groningen), Cynthia J. Curry(University Medical Center Groningen), Arnd Dörfler(University Medical Center Groningen), Detlev Schindler(University of Würzburg), Helmuth‐Günther Dörr(University Medical Center Groningen), Bruno Dallapiccola(Bambino Gesù Children's Hospital)
Cited by 397
Related Papers
Abnormal Behavior Associated with a Point Mutation in the Structural Gene for Monoamine Oxidase A
|Science|1993|1.6k
Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.
|Journal of Medical Genetics|1997|1.2k