Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
Journal
The American Journal of Human Genetics
ISSN
0002-9297
Date Issued
2020
Author(s)
Yingjie Zhao
Alexander Diacou
H. Richard Johnston
Fadi I. Musfee
Donna M. McDonald-McGinn
Daniel McGinn
T. Blaine Crowley
Ann Swillen
Jeroen Breckpot
Joris R. Vermeesch
Wendy R. Kates
M. Cristina Digilio
Marta Unolt
Bruno Marino
Maria Pontillo
Marco Armando
Fabio Di Fabio
Stefano Vicari
Marianne van den Bree
Hayley Moss
Michael J. Owen
Kieran C. Murphy
Clodagh M. Murphy
Declan Murphy
Kelly Schoch
Vandana Shashi
Flora Tassone
Tony J. Simon
Robert J. Shprintzen
Linda Campbell
Nicole Philip
Damian Heine-Suñer
Sixto García-Miñaúr
Luis Fernández
Carrie E. Bearden
Claudia Vingerhoets
Therese van Amelsvoort
Stephan Eliez
Maude Schneider
Jacob A.S. Vorstman
Doron Gothelf
Elaine Zackai
A.J. Agopian
Raquel E. Gur
Anne S. Bassett
Beverly S. Emanuel
Elizabeth Goldmuntz
Laura E. Mitchell
Tao Wang
Bernice E. Morrow
Stylianos E. Antonarakis
Massimo Biondi
Erik Boot
Elemi Breetvelt
Tiffany Busa
Nancy Butcher
Antonino Buzzanca
Miri Carmel
Isabelle Cleynen
David Cutler
Bruno Dallapiccola
María Angeles de la Fuente Sanches
Michael P. Epstein
Rens Evers
Luis Fernandez
Rosemarie Fritsch
Fernando García Algas
Tingwei Guo
Raquel Gur
Matthew S. Hestand
Tracy Heung
Stephen Hooper
Andrea Jin
Leila Kushan-Wells
Alejandra Teresa Laorden-Nieto
Guido Lattanzi
Christian Marshall
Kathryn McCabe
Elena Michaelovsky
Claudia Ornstein
Candice Silversides
Oanh Tran
Esther D.A. van Duin
Elfi Vergaelen
Steve T. Warren
Ronnie Weinberger
Abraham Weizman
Zhengdong Zhang
Michael Zwick
Type
Resource Types::text::journal::journal article
DOI
URL