Work

Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B

Year: 2000

Type: article

Study design: Observational Study

Source: Nature Genetics

DOI: 10.1038/73495

Authors: Michael Oldridge, Ana M Fortuna, Monika Maringa, Peter Propping, Sahar Mansour, Christine Pollitt, Thomas M. DeChiara, Robert B. Kimble, David M. Valenzuela, George D. Yancopoulos, Andrew O.M. Wilkie

Institutions: John Radcliffe Hospital, University of Oxford, University of Bonn, St George's, University of London, Royal Victoria Infirmary, Regeneron (United States)

Language: English

Topic: Congenital limb and hand anomalies

Subfield: Developmental Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W1974032064

FWCI: 16.16

Cites: 21

Cited by: 234

Related to: 10