Work

Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment

Year: 1983

Type: article

Study design: Case Report

Source: Human Genetics

DOI: 10.1007/bf00292373

Authors: M. Fraccaro, O. Zuffardi, E. B�hler, A. Schinzel, G. Simoni, R. Witkowski, E. Bonifaci, D. Caufin, G. Cignacco, N. Delendi, L. Gargantini, T. Losanowa, L. Marca, E. Ullrich, V. Vigi

Institutions: University of Pavia, University of Zurich, University of Milan, Humboldt-Universität zu Berlin, Charité – Universitätsmedizin Berlin, Azienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda, University of Ferrara

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: green

OpenAlex ID: W1998344508

FWCI: 4.711

Cites: 23

Cited by: 49

Related to: 10