- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1750-1172
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
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
- Creator
-
Negishi, Yutaka
Ieda, Daisuke
Hori, Ikumi
Nozaki, Yasuyuki
Yamagata, Takanori
Komaki, Hirofumi
Tohyama, Jun
Nagasaki, Keisuke
Tada, Hiroko
Saitoh, Shinji
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s13023-019-1249-4
- URN
-
urn:nbn:de:101:1-2020032522451376739487
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 11:00 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- 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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Orthopedic manifestations in children with Prader-Willi syndrome
Distinct promoter regions of the oxytocin receptor gene are hypomethylated in Prader-Willi syndrome and in Prader-Willi syndrome associated psychosis
Incidence of strabismus, strabismus surgeries, and other vision conditions in Prader-Willi syndrome: data from the Global Prader-Willi Syndrome Registry
The Italian registry for patients with Prader–Willi syndrome
Aripiprazole treatment for temper outbursts in Prader–Willi syndrome
Management of Prader-Willi syndrome
Management of Prader-Willi syndrome
Sleep Consequences of Prader-Willi Syndrome
Ovarian cyst torsion in Prader-Willi Syndrome
Prader-Willi syndrome: A primer for clinicians
The Prader-Willi syndrome Profile: validation of a new measure of behavioral and emotional problems in Prader-Willi syndrome
Prader-Willi syndrome : selected research and management issues
Orthopedic manifestations in children with Prader-Willi syndrome
Distinct promoter regions of the oxytocin receptor gene are hypomethylated in Prader-Willi syndrome and in Prader-Willi syndrome associated psychosis
Incidence of strabismus, strabismus surgeries, and other vision conditions in Prader-Willi syndrome: data from the Global Prader-Willi Syndrome Registry
The Italian registry for patients with Prader–Willi syndrome