Diagnostics of rare disorders: whole-exome sequencing deciphering locus heterogeneity in telomere biology disorders
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1750-1172
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
-
online resource.
- Erschienen in
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Diagnostics of rare disorders: whole-exome sequencing deciphering locus heterogeneity in telomere biology disorders ; volume:13 ; number:1 ; day:17 ; month:8 ; year:2018 ; pages:1-9 ; date:12.2018
Orphanet journal of rare diseases ; 13, Heft 1 (17.8.2018), 1-9, 12.2018
- Urheber
-
Trotta, Luca
- Beteiligte Personen und Organisationen
-
Norberg, Anna
Taskinen, Mervi
Béziat, Vivien
Degerman, Sofie
Wartiovaara-Kautto, Ulla
Välimaa, Hannamari
Jahnukainen, Kirsi
Casanova, Jean-Laurent
Seppänen, Mikko
Saarela, Janna
Koskenvuo, Minna
Martelius, Timi
SpringerLink (Online service)
- DOI
-
10.1186/s13023-018-0864-9
- URN
-
urn:nbn:de:101:1-2018090310135741297289
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
- 15.08.2025, 07:25 MESZ
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Beteiligte
- Trotta, Luca
- Norberg, Anna
- Taskinen, Mervi
- Béziat, Vivien
- Degerman, Sofie
- Wartiovaara-Kautto, Ulla
- Välimaa, Hannamari
- Jahnukainen, Kirsi
- Casanova, Jean-Laurent
- Seppänen, Mikko
- Saarela, Janna
- Koskenvuo, Minna
- Martelius, Timi
- SpringerLink (Online service)
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