WDR26 Haploinsufficiency Causes a Recognizable Syndrome of Intellectual Disability, Seizures, Abnormal Gait, and Distinctive Facial Features
Cara Skraban(Children's Hospital of Philadelphia), Matthew A. Deardorf, Rolph Pfundt(Radboud University Nijmegen), Alice Goldenberg(Université de Rouen Normandie), Lynne M. Bird(University of California San Diego), Ping Yee Billie Au(University of Calgary), Stephen P. Robertson(University of Otago), Taylor Warner(University of Iowa), Arjan P.M. de Brouwer(Radboud University Nijmegen), Patricia G. Wheeler(Nemours Children's Clinic), Amber Stocco(INTEGRIS Baptist Medical Center), Avni Santani(Children's Hospital of Philadelphia), Evelien Zonneveld‐Huijssoon(University Medical Center Groningen), Marlies Kempers(Radboud University Nijmegen), Koen L.I. van Gassen(University Medical Center Utrecht), Amber Begtrup, Claire Turner(Royal Devon and Exeter Hospital), John Bernat(University of Iowa Stead Family Children’s Hospital), Elizabeth H. Denenberg(Children's Hospital of Philadelphia), Kristin McDonald Gibson(Children's Hospital of Philadelphia), Ganka Douglas, A. Micheil Innes(University of Calgary), Laurence E. Walsh(Indiana University Health), Dagmar Wieczorek(Essen University Hospital), Jane Juusola, Esther Kinning(University Medical Center Groningen), Megan T. Cho, David Markie(Mount Sinai Hospital), Constance Wells(Génétique Médicale & Génomique Fonctionelle), Martina Owens(Royal Devon & Exeter NHS Foundation Trust), Katheryn Grand(Cedars-Sinai Medical Center), Tjitske Kleefstra(Radboud University Nijmegen), Ka–Jia Cao(Children's Hospital of Philadelphia), Katelyn Payne(Indiana University Health), Deciphering Developmental Disorders Study, Nienke E. Verbeek(University Medical Center Utrecht), Alisha Wilkens(Children's Hospital of Philadelphia), Addie I. Nesbitt(Children's Hospital of Philadelphia), Richard Person(GenVec), Preetha Markose(Children's Hospital of Philadelphia)
Utrecht University Repository (Utrecht University)
July 6, 2017
Cited by 0
Related Papers
Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian Disorders
|New England Journal of Medicine|2013|2k