Work

Uniparental disomy as a mechanism for human genetic disease.

Year: 1988

Type: article

Study design: Case Report

Source: PubMed

Authors: J E Spence, R G Perciaccante, G M Greig, H F Willard, D H Ledbetter, J F Hejtmancik, M S Pollack, W E O'Brien, A L Beaudet

Institution: Baylor College of Medicine

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

OpenAlex ID: W1588409425

FWCI: 8.524

Cites: 38

Cited by: 486

Related to: 10