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
Publication title -
obm genetics
Language(s) - English
Resource type - Journals
ISSN - 2577-5790
DOI - 10.21926/obm.genet.1801015
Subject(s) - hypotonia , medicine , pediatrics , genetic testing , differential diagnosis , neonatal intensive care unit , intensive care , bioinformatics , intensive care medicine , pathology , biology
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