Hochschulschrift
Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Erschienen in
-
In: 10.1186/s13148-020-00856-y
- Ereignis
-
Veröffentlichung
- (wo)
-
Aachen
- (wer)
-
Universitätsbibliothek der RWTH Aachen
- (wann)
-
2020
- Urheber
-
Eßinger, Carla
Karch, Stephanie
Moog, Ute
Fekete, György
Lengyel, Anna
Pinti, Eva
Eggermann, Thomas
Begemann, Matthias
- DOI
-
10.18154/RWTH-CONV-243322
- URN
-
urn:nbn:de:101:1-2023040505583040055038
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 11:01 MESZ
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Objekttyp
- Hochschulschrift
Beteiligte
- Eßinger, Carla
- Karch, Stephanie
- Moog, Ute
- Fekete, György
- Lengyel, Anna
- Pinti, Eva
- Eggermann, Thomas
- Begemann, Matthias
- Universitätsbibliothek der RWTH Aachen
Entstanden
- 2020
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