Work

Equal parental origin of chromosome 22 losses in human sporadic meningioma: no evidence for genomic imprinting.

Year: 1990

Type: article

Source: PubMed

Authors: B Fontaine, G A Rouleau, B Seizinger, A F Jewell, M P Hanson, R L Martuza, J F Gusella

Institution: Massachusetts General Hospital

Language: English

Topic: Genetic Syndromes and Imprinting

Subfield: Genetics

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 Neurological Disorders and Stroke

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

OpenAlex ID: W1492883792

FWCI: 1.461

Cites: 25

Cited by: 11

Related to: 10