Work

Expanding the clinical history associated with syndromic Klippel-Feil: A unique case of comorbidity with medulloblastoma

Year: 2019

Type: article

Study design: Case Report

Source: European Journal of Medical Genetics

DOI: 10.1016/j.ejmg.2019.103701

Authors: Kathleen M. Schieffer, Elizabeth Varga, Katherine E. Miller, Vibhuti Agarwal, Daniel C. Koboldt, Patrick Brennan, Benjamin Kelly, Ashita Dave-Wala, Christopher R. Pierson, Jonathan L. Finlay, Mohamed S. AbdelBaki, Peter White, Vincent Magrini, Richard K. Wilson, Elaine R. Mardis, Catherine E. Cottrell

Institutions: Nationwide Children's Hospital, The Ohio State University

Language: English

Topic: Genomics and Rare Diseases

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funders: University of California, Santa Cruz, Research Institute, Nationwide Children's Hospital, National Cancer Institute

Award: Cancer Center Support Grant

OpenAlex ID: W2952416712

FWCI: 1.08

Cites: 27

Cited by: 17

Related to: 10