Work

Parental origin of chromosome 22 loss in sporadic and NF2 neuromas

Year: 1991

Type: article

Study design: Observational Study

Source: Genomics

DOI: 10.1016/0888-7543(91)90513-e

Authors: Bertrand Fontaine, Marc Sanson, Olivier Delattre, Anil G. Menon, Guy A. Rouleau, Bernd R. Seizinger, Ann F. Jewell, Mark P. Hanson, Alain Aurias, Robert L. Martuza, James F. Gusella, Gilles Thomas

Institutions: Harvard University, Massachusetts General Hospital, Centre National de la Recherche Scientifique, Institut Curie, Montreal General Hospital, McGill University

Language: English

Topic: Neurofibromatosis and Schwannoma Cases

Subfield: Neurology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Institute of Neurological Disorders and Stroke

Awards: REFERENCE PEDIGREES FOR HUMAN GENETIC LINKAGE ANALYSIS, GENETIC AND MOLECULAR STUDIES OF NEUROFIBROMATOSIS 1, G394857964, Molecular Genetics of Inherited Neurological Diseases, G793505578, G810187598

OpenAlex ID: W2139557688

FWCI: 4.674

Cites: 35

Cited by: 21

Related to: 10