Work

Uncommon Deletions of the Smith-Magenis Syndrome Region Can Be Recurrent When Alternate Low-Copy Repeats Act as Homologous Recombination Substrates

Year: 2004

Type: article

Source: The American Journal of Human Genetics

DOI: 10.1086/422016

Authors: Christine J. Shaw, Marjorie A. Withers, James R. Lupski

Institutions: Baylor College of Medicine, 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: bronze

Funders: National Institutes of Health, National Institute of Child Health and Human Development, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Awards: G2156526443, G2516091520, Chromosome Rearrangements and Mental Retardation, Baylor Intellectual and Developmental Disabilities Research Center

OpenAlex ID: W2053290166

FWCI: 6.069

Cites: 40

Cited by: 62

Related to: 10