Work

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

Year: 1995

Type: article

Study design: Observational Study

Source: Nature Genetics

DOI: 10.1038/ng0295-165

Authors: Andrew O.M. Wilkie, Sarah F. Slaney, Michael Oldridge, Michael D. Poole, Geraldine J. Ashworth, Anthony D. Hockley, Richard D. Hayward, David J. David, Louise J. Pulleyn, Paul Rutland, Susan Malcolm, Robin M. Winter, William Reardon

Institutions: John Radcliffe Hospital, University of Oxford, Churchill Hospital, Queen Elizabeth Hospital Birmingham, Great Ormond Street Hospital, Great Ormond Street Hospital for Children NHS Foundation Trust, Women's and Children's Hospital

Language: English

Topic: Craniofacial Disorders and Treatments

Subfield: Surgery

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Wellcome Trust

OpenAlex ID: W2067732333

FWCI: 81.55

Cites: 71

Cited by: 939

Related to: 10