Work

The Breakpoint Region of the Most Common Isochromosome, i(17q), in Human Neoplasia Is Characterized by a Complex Genomic Architecture with Large, Palindromic, Low-Copy Repeats

Year: 2004

Type: article

Source: The American Journal of Human Genetics

DOI: 10.1086/380648

Authors: Aikaterini Barbouti, Pawel Stankiewicz, Chad Nusbaum, Christina Cuomo, April Cook, Mattias Höglund, Bertil Johansson, Anne Hagemeijer, Sung-Sup Park, Felix Mitelman, James R. Lupski, Thoas Fioretos

Institutions: Lund University, Whitehead Institute for Biomedical Research, Massachusetts Institute of Technology, KU Leuven, 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: Swedish Cancer Foundation, Cancerfonden, National Institutes of Health, National Institute of Child Health and Human Development, Eunice Kennedy Shriver National Institute of Child Health and Human Development

Award: Chromosome Rearrangements and Mental Retardation

OpenAlex ID: W2033715497

FWCI: 8.032

Cites: 40

Cited by: 128

Related to: 10