Work

Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion in one family

Year: 1995

Type: article

Study design: Observational Study

Source: Human Molecular Genetics

DOI: 10.1093/hmg/4.1.71

Authors: S. Mundlos, J. B. Mulliken, D. L. Abramsom, M. L. Warman, J. H. M. Knoll, B. R. Olsen

Institutions: Boston Children's Hospital, Harvard University

Language: English

Topic: dental development and anomalies

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Institute of Arthritis and Musculoskeletal and Skin Diseases

Awards: G118651670, G475519389

OpenAlex ID: W2008240965

FWCI: 2.354

Cites:

Cited by: 117

Related to: 10