학술논문
Exome sequencing identifies variants in infants with sacral agenesis.
Document Type
Article
Author
Pitsava, Georgia; Feldkamp, Marcia L.; Pankratz, Nathan; Lane, John; Kay, Denise M.; Conway, Kristin M.; Hobbs, Charlotte; Shaw, Gary M.; Reefhuis, Jennita; Jenkins, Mary M.; Almli, Lynn M.; Moore, Cynthia; Werler, Martha; Browne, Marilyn L.; Cunniff, Chris; Olshan, Andrew F.; Pangilinan, Faith; Brody, Lawrence C.; Sicko, Robert J.; Finnell, Richard H.
Source
Birth Defects Research; Apr2022, Vol. 114 Issue 7, p215-227, 13p
Subject
Language
ISSN
24721727
Abstract
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