De novo POGZ mutations are associated with neurodevelopmental disorders and microcephaly.

Ye, Yizhou; Cho, Megan T; Retterer, Kyle; Alexander, Nora; Ben-Omran, Tawfeg; Al-Mureikhi, Mariam; Cristian, Ingrid; Wheeler, Patricia G; Crain, Carrie; Zand, Dina; Weinstein, Veronique; Vernon, Hilary J; McClellan, Rebecca; Krishnamurthy, Vidya; Vitazka, Patrik; Millan, Francisca; Chung, Wendy K.

Afiliação

Ye Y; GeneDx, Gaithersburg, Maryland 20877, USA;
Cho MT; GeneDx, Gaithersburg, Maryland 20877, USA;
Retterer K; GeneDx, Gaithersburg, Maryland 20877, USA;
Alexander N; GeneDx, Gaithersburg, Maryland 20877, USA;
Ben-Omran T; Clinical and Metabolic Genetics, Hamad Medical Corporation, Doha, Qatar;
Al-Mureikhi M; Clinical and Metabolic Genetics, Hamad Medical Corporation, Doha, Qatar;
Cristian I; Nemours Children's Hospital, Orlando, Florida 32827, USA;
Wheeler PG; Nemours Children's Hospital, Orlando, Florida 32827, USA;
Crain C; Nemours Children's Hospital, Orlando, Florida 32827, USA;
Zand D; Children's National Medical Center, Washington, D.C. 20010, USA;
Weinstein V; Children's National Medical Center, Washington, D.C. 20010, USA;
Vernon HJ; Kennedy Krieger Institute, Baltimore, Maryland 21205, USA;
McClellan R; Kennedy Krieger Institute, Baltimore, Maryland 21205, USA;
Krishnamurthy V; Pediatrics and Genetics, Alpharetta, Georgia 30005, USA;
Vitazka P; GeneDx, Gaithersburg, Maryland 20877, USA;
Millan F; GeneDx, Gaithersburg, Maryland 20877, USA;
Chung WK; Departments of Pediatrics and Medicine, Columbia University Medical Center, New York, New York 10032, USA.