Open AccessApplication of Clinical Next Generation Sequencing in Intensive Care Facilitates Rapid Diagnosis of Neonates with Rare Genetic Disorders
Author(s) -
Tobias Geis,
Ute Hehr,
Roland Brandl,
Saskia M. Herbst,
Hugo Segerer,
Michael Melter,
Sophie Hinreiner
Publication year - 2018
Language(s) - English
DOI - 10.21926/obm.genet.1801015
Subject(s) - hypotonia , medicine , genetic testing , pediatrics , differential diagnosis , neonatal intensive care unit , intensive care , bioinformatics , intensive care medicine , pathology , biology