Skip to content Skip to footer

Research Portal of the TU Dresden

A further example of the role of small non-coding RNAs (sncRNAs) in syndromic diseases that also highlights the diagnostic gap of Whole Exome Sequencing (WES)

Research output: Contribution to book/Conference proceedings/Anthology/Report › Other chapter contribution › Contributed › peer-review

Contributors

Sylvia Hütter - , Institute of Clinical Genetics (Author)
Marie Arlt - , Institute of Clinical Genetics (Author)
Karl Hackmann - , Institute of Clinical Genetics (Author)
Doreen William - , Institute of Clinical Genetics (Author)
Oliver Kutz - , Institute of Clinical Genetics (Author)
Tim Hutschenreiter - , Institute of Clinical Genetics (Author)
Franziska Steinz - , Institute of Clinical Genetics (Author)
Tanita Kretschmer - (Author)
Andreas Dahl - , DRESDEN-concept Genome Center (CMCB Core Facility) (Author)
Jens Christoph Schallner - , Department of Paediatrics, Social Pediatric Center (Author)
Evelin Schröck - , Institute of Clinical Genetics (Author)
Joseph Porrmann - , Institute of Clinical Genetics (Author)

Details

Original language	English
Title of host publication	A further example of the role of small non-coding RNAs (sncRNAs) in syndromic diseases that also highlights the diagnostic gap of Whole Exome Sequencing (WES)
Publication status	Published - 2024
Peer-reviewed	Yes

Keywords