De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 Deletions.
Brieana Fregeau,Bum Jun Kim,Andrés Hernández-García,Valerie K Jordan,Megan T Cho,Rhonda E Schnur,Kristin G Monaghan,Jane Juusola,Jill A Rosenfeld,Elizabeth Bhoj,Elaine H Zackai,Stephanie Sacharow,Kristin Barañano,Daniëlle G M Bosch,Bert B A de Vries,Kristin Lindstrom,Audrey Schroeder,Philip James,Peggy Kulch,Seema R Lalani,Mieke M van Haelst,Koen L I van Gassen,Ellen van Binsbergen,A James Barkovich,Daryl A Scott,Elliott H Sherr American journal of human genetics（2016）
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