Work

Haplotype analysis of two recurrent CDKN2A mutations in 10 melanoma families: Evidence for common founders and independent mutations

Year: 1998

Type: article

Study design: Observational Study

Source: Human Mutation

DOI: 10.1002/(sici)1098-1004(1998)11:6<424::aid-humu2>3.0.co;2-2

Authors: Pamela M. Pollock, Nigel Spurr, Tim Bishop, Julia Newton-Bishop, Nelleke Gruis, Pieter A. van der Velden, Alisa M. Goldstein, Margaret A. Tucker, William D. Foulkes, Ray Barnhill, Daniel Haber, Jane Fountain, Nicholas K. Hayward

Institutions: QIMR Berghofer Medical Research Institute, St James's University Hospital, Leiden University Medical Center, National Cancer Institute, McGill University, Brigham and Women's Hospital, Harvard University, Massachusetts General Hospital, University of Southern California

Language: English

Topic: Cutaneous Melanoma Detection and Management

Subfield: Oncology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: Cancer Research Society, National Institutes of Health, National Health and Medical Research Council, National Medical Research Council, National Cancer Institute

Awards: UNRAVELING THE ROLE OF 9P21 GENE MUTATIONS IN MELANOMA, G8776205327

OpenAlex ID: W1986540282

FWCI: 2.671

Cites: 41

Cited by: 62

Related to: 10