Work

Imprinting mutations in the Beckwith—Wiedemann syndrome suggested by an altered imprinting pattern in the IGF2–H19 domain

Year: 1995

Type: article

Source: Human Molecular Genetics

DOI: 10.1093/hmg/4.12.2379

Authors: Wolf Reik, Keith W. Brown, Helene Schneid, Yves Le Bouc, Wendy Bickmore, Eamonn R. Maher

Institutions: Babraham Institute, University of Bristol, Hôpital Armand-Trousseau, MRC Human Genetics Unit, University of Cambridge, Addenbrooke's Hospital

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

Funder: Wellcome Trust

OpenAlex ID: W2105650844

FWCI: 7.743

Cites:

Cited by: 220

Related to: 10