Work

A Physical Map of the Mouseshaker-2Region Contains Many of the Genes Commonly Deleted in Smith–Magenis Syndrome (del17p11.2p11.2)

Year: 1999

Type: article

Source: Genomics

DOI: 10.1006/geno.1998.5669

Authors: Frank J. Probst, Ken-Shiung Chen, Qi Zhao, Aihui Wang, Thomas B. Friedman, James R. Lupski, Sally A. Camper

Institutions: University of Michigan, Baylor College of Medicine, National Institutes of Health, National Institute on Deafness and Other Communication Disorders, Michigan State University, Texas Children's Hospital

Language: English

Topic: Genomic variations and chromosomal abnormalities

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 on Deafness and Other Communication Disorders, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G3689424842, G5441383957, A Panhypopituitary Mouse Mutation, Mapping And Cloning Hereditary Hearing Impairment Genes, Positional Cloning of DFNB3 Reveals a Novel Unconventional Myosin, MYO15, G815524270

OpenAlex ID: W2016169728

FWCI: 1.584

Cites:

Cited by: 29

Related to: 10