Work

A Novel, Single Nucleotide Polymorphism-Based Assay to Detect 22q11 Deletions

Year: 2007

Type: article

Source: Genetic Testing

DOI: 10.1089/gte.2006.0507

Authors: Birgit H. Funke, Alison C. Brown, Marco F. Ramoni, Maura E. Regan, Chris Baglieri, Christine T. Finn, Melanie Babcock, Robert J. Shprintzen, Bernice E. Morrow, Raju Kucherlapati

Institutions: Harvard University, Yeshiva University, Harvard–MIT Division of Health Sciences and Technology, Massachusetts Institute of Technology, Albert Einstein College of Medicine, SUNY Upstate Medical University

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

Award: G719145235

OpenAlex ID: W2070993127

FWCI: 0.536

Cites: 45

Cited by: 7

Related to: 10