Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome-Reference-Cited by-同舟云学术

Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome

Published:2015-05 Issue:5 Volume:96 Page:753-764
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Mlynarski Elisabeth E.,Sheridan Molly B.,Xie Michael,Guo Tingwei,Racedo Silvia E.,McDonald-McGinn Donna M.,Gai Xiaowu,Chow Eva W.C.,Vorstman Jacob,Swillen Ann,Devriendt Koen,Breckpot Jeroen,Digilio Maria Cristina,Marino Bruno,Dallapiccola Bruno,Philip Nicole,Simon Tony J.,Roberts Amy E.,Piotrowicz Małgorzata,Bearden Carrie E.,Eliez Stephan,Gothelf Doron,Coleman Karlene,Kates Wendy R.,Devoto Marcella,Zackai Elaine,Heine-Suñer Damian,Shaikh Tamim H.,Bassett Anne S.,Goldmuntz Elizabeth,Morrow Bernice E.,Emanuel Beverly S.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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