Improved Diagnosis of Rare Disease Patients through Systematic Detection of Runs of Homozygosity

Matalonga, Leslie; Laurie, Steven; Papakonstantinou, Anastasios; Piscia, Davide; Mereu, Elisabetta; Bullich, Gemma; Thompson, Rachel; Horvath, Rita; Perez-Jurado, Luis; Riess, Olaf; Gut, Ivo; van Ommen, Gert-Jan; Lochmueller, Hanns; Beltran, Sergi

dc.contributor.author	Rieß, Olaf
dc.date.accessioned	2021-06-15T10:32:22Z
dc.date.available	2021-06-15T10:32:22Z
dc.date.issued	2020
dc.identifier.issn	1943-7811
dc.identifier.uri	http://hdl.handle.net/10900/116311
dc.language.iso	en	de_DE
dc.publisher	Elsevier Science Inc	de_DE
dc.relation.uri	http://dx.doi.org/10.1016/j.jmoldx.2020.06.008	de_DE
dc.subject.ddc	610	de_DE
dc.title	Improved Diagnosis of Rare Disease Patients through Systematic Detection of Runs of Homozygosity	de_DE
dc.type	Article	de_DE
utue.quellen.id	20210304112512_01692
utue.publikation.seiten	1205-1215	de_DE
utue.personen.roh	Matalonga, Leslie
utue.personen.roh	Laurie, Steven
utue.personen.roh	Papakonstantinou, Anastasios
utue.personen.roh	Piscia, Davide
utue.personen.roh	Mereu, Elisabetta
utue.personen.roh	Bullich, Gemma
utue.personen.roh	Thompson, Rachel
utue.personen.roh	Horvath, Rita
utue.personen.roh	Perez-Jurado, Luis
utue.personen.roh	Riess, Olaf
utue.personen.roh	Gut, Ivo
utue.personen.roh	van Ommen, Gert-Jan
utue.personen.roh	Lochmueller, Hanns
utue.personen.roh	Beltran, Sergi
dcterms.isPartOf.ZSTitelID	Journal of Molecular Diagnostics	de_DE
dcterms.isPartOf.ZS-Issue	9	de_DE
dcterms.isPartOf.ZS-Volume	22	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE