Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci
- 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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Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci ; volume:7 ; number:1 ; day:14 ; month:11 ; year:2015 ; pages:1-18 ; date:12.2015
Clinical epigenetics ; 7, Heft 1 (14.11.2015), 1-18, 12.2015
- Urheber
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Eggermann, Thomas
- Beteiligte Personen und Organisationen
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Perez de Nanclares, Guiomar
Maher, Eamonn R.
Temple, I. Karen
Tümer, Zeynep
Monk, David
Mackay, Deborah J. G.
Grønskov, Karen
Riccio, Andrea
Linglart, Agnès
Netchine, Irène
SpringerLink (Online service)
- DOI
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10.1186/s13148-015-0143-8
- URN
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urn:nbn:de:1111-2016030830295
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:22 MESZ
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Beteiligte
- Eggermann, Thomas
- Perez de Nanclares, Guiomar
- Maher, Eamonn R.
- Temple, I. Karen
- Tümer, Zeynep
- Monk, David
- Mackay, Deborah J. G.
- Grønskov, Karen
- Riccio, Andrea
- Linglart, Agnès
- Netchine, Irène
- SpringerLink (Online service)
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Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure
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Unusual deletion of the maternal 11p15 allele in Beckwith-Wiedemann syndrome with an impact on both imprinting domains
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