Schaaf-Yang syndrome shows a Prader-Willi syndrome-like phenotype during infancy
- 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
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online resource.
- Erschienen in
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Schaaf-Yang syndrome shows a Prader-Willi syndrome-like phenotype during infancy ; volume:14 ; number:1 ; day:2 ; month:12 ; year:2019 ; pages:1-7 ; date:12.2019
Orphanet journal of rare diseases ; 14, Heft 1 (2.12.2019), 1-7, 12.2019
- Urheber
-
Negishi, Yutaka
Ieda, Daisuke
Hori, Ikumi
Nozaki, Yasuyuki
Yamagata, Takanori
Komaki, Hirofumi
Tohyama, Jun
Nagasaki, Keisuke
Tada, Hiroko
Saitoh, Shinji
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1186/s13023-019-1249-4
- URN
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urn:nbn:de:101:1-2020032522451376739487
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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14.08.2025, 11:00 MESZ
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Beteiligte
- Negishi, Yutaka
- Ieda, Daisuke
- Hori, Ikumi
- Nozaki, Yasuyuki
- Yamagata, Takanori
- Komaki, Hirofumi
- Tohyama, Jun
- Nagasaki, Keisuke
- Tada, Hiroko
- Saitoh, Shinji
- SpringerLink (Online service)
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Distinct promoter regions of the oxytocin receptor gene are hypomethylated in Prader-Willi syndrome and in Prader-Willi syndrome associated psychosis
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The Italian registry for patients with Prader–Willi syndrome
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