Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1868-7083
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome ; volume:12 ; number:1 ; day:11 ; month:5 ; year:2020 ; pages:1-7 ; date:12.2020
Clinical epigenetics ; 12, Heft 1 (11.5.2020), 1-7, 12.2020
- Urheber
-
Eßinger, Carla
Karch, Stephanie
Moog, Ute
Fekete, György
Lengyel, Anna
Pinti, Eva
Eggermann, Thomas
Begemann, Matthias
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
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10.1186/s13148-020-00856-y
- URN
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urn:nbn:de:101:1-2020071707283530001598
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 11:00 MESZ
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Beteiligte
- Eßinger, Carla
- Karch, Stephanie
- Moog, Ute
- Fekete, György
- Lengyel, Anna
- Pinti, Eva
- Eggermann, Thomas
- Begemann, Matthias
- SpringerLink (Online service)
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