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Xp21 contiguous gene syndromes: deletion quantitation with bivariate flow karyotyping allows mapping of patient breakpoints.

PubMed

Year: 1992
Type: article
Study design: Observational Study
Source: PubMed
Authors: E R McCabe, J A Towbin, G van den Engh, B J Trask
Institution: Baylor College of Medicine
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: green

Funders: National Heart, Lung, and Blood Institute, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: MOLECULAR GENETIC STUDIES OF GLYCEROL KINASE DEFICIENCY, MOLECULAR LINKAGE AND CLONING OF X-LINKED CARDIOMYOPATHY, Baylor Intellectual and Developmental Disabilities Research Center
OpenAlex ID: W1504866013
FWCI: 0.844
Cites: 37
Cited by: 21
Related to: 10
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