Work

Clinical utility gene card for: Prader-Willi Syndrome

Year: 2014

Type: article

Source: European Journal of Human Genetics

DOI: 10.1038/ejhg.2014.66

Authors: Karin Buiting, Suzanne B Cassidy, Daniel J Driscoll, Gabriele Gillessen-Kaesbach, Deniz Kanber, Maithé Tauber, Eberhard Schwinger, Bernhard Horsthemke

Institutions: Essen University Hospital, University of Duisburg-Essen, University of California, San Francisco, University of Florida Health, University of Florida, University of Lübeck, Inserm, Centre Hospitalier Universitaire de Toulouse, Centre de Physiopathologie de Toulouse-Purpan, Hôpital des Enfants

Language: English

Topic: Genetic Syndromes and Imprinting

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: European Commission, Bundesministerium für Bildung und Forschung, National Institute of General Medical Sciences

Awards: Genetic testing in Europe - Network for the further development, harmonization, validation and standardization of services, G8636574975

OpenAlex ID: W2031821698

FWCI: 0.876

Cites: 4

Cited by: 21

Related to: 10