Refining analyses of copy number variation identifies specific genes associated with developmental delay
Bradley P. Coe(University of Washington), Kali Witherspoon(University of Washington), Jill A. Rosenfeld(PerkinElmer (United States)), Bregje W.M. van Bon(Radboud University Nijmegen), Anneke T. Vulto‐van Silfhout(Radboud University Nijmegen), Paolo Bosco(Oasi Maria SS), Kathryn Friend(South Australia Pathology), Carl Baker(University of Washington), Serafino Buono(Oasi Maria SS), Lisenka E.L.M. Vissers(Radboud University Nijmegen), Janneke Schuurs-Hoeijmakers(Radboud University Nijmegen), Alexander Hoischen(Radboud University Nijmegen), Rolph Pfundt(Radboud University Nijmegen), Nik Krumm(University of Washington), Gemma L. Carvill(University of Washington), Deana Li(Autism Research Institute), David G. Amaral(Autism Research Institute), Natasha J. Brown(Barwon Health), Paul J. Lockhart(Royal Children's Hospital), Ingrid E. Scheffer(Royal Children's Hospital), A Alberti(Oasi Maria SS), Marie Shaw(South Australia Pathology), Rosa Pettinato(Oasi Maria SS), Raymond C. Tervo(Mayo Clinic), Nicole de Leeuw(Radboud University Nijmegen), Margot R.F. Reijnders(Radboud University Nijmegen), Beth S. Torchia(PerkinElmer (United States)), Hilde Peeters(Center for Human Genetics), Elizabeth Thompson(South Australia Pathology), Brian J. O’Roak(University of Washington), Marco Fichera(Radboud University Nijmegen), Jayne Y. Hehir‐Kwa(Radboud University Nijmegen), Jay Shendure(University of Washington), Heather C. Mefford(University of South Australia), Eric Haan(South Australia Pathology), Jozef Gécz(South Australia Pathology), Bert B A de Vries(Radboud University Nijmegen), Corrado Romano(Howard Hughes Medical Institute), Evan E Eichler(Howard Hughes Medical Institute)
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