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Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes
Author(s) -
Maria Delio,
Tingwei Guo,
Donna M. McDonaldMcGinn,
Elaine H. Zackai,
Sean Herman,
Mark Kaminetzky,
Anne Marie Higgins,
Karlene Coleman,
Carolyn Chow,
Maria Jarlbrzkowski,
Carrie Bearden,
Alice A. Bailey,
Anders Vangkilde,
Line Olsen,
Charlotte Olesen,
Flemming Skovby,
Thomas Werge,
Ludivine Templin,
Tiffany Busa,
Nicole Philip,
Ann Swillen,
Joris Vermeesch,
Koen Devriendt,
Maude Schneider,
Sophie Dahoun,
Stéphan Eliez,
Kelly Schoch,
Stephen R. Hooper,
Vandana Shashi,
Joy Samanich,
Robert W. Marion,
Thérèse van Amelsvoort
Publication year - 2013
Publication title -
carolina digital repository (university of north carolina at chapel hill)
Language(s) - English
DOI - 10.17615/86qc-4989
Subject(s) - digeorge syndrome , genetics , biology , medicine

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