Work

Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

Year: 1989

Type: article

Source: American Journal of Medical Genetics

DOI: 10.1002/ajmg.1320320235

Authors: J. H. M. Knoll, R. D. Nicholls, R. E. Magenis, J. M. Graham, M. Lalande, S. A. Latt, John M. Opitz, James F. Reynolds

Institutions: Boston Children's Hospital, Howard Hughes Medical Institute, Harvard University, Oregon Health & Science University, Cedars-Sinai Medical Center, University of California, Los Angeles

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: closed

Funders: National Institutes of Health, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Award: G689141124

OpenAlex ID: W2043882061

FWCI: 22.65

Cites: 19

Cited by: 576

Related to: 10