PubMed:1776638 JSONTXT

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{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/1776638","sourcedb":"PubMed","sourceid":"1776638","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/1776638","text":"Gardner syndrome in a boy with interstitial deletion of the long arm of chromosome 5.\nWe described a 15-year-old boy with Gardner syndrome (GS), mental retardation, and craniofacial abnormalities. High-resolution banding analysis showed an interstitial deletion of the long arm of chromosome 5 (q22.1----q31.1). The breakpoints in the present case and in 3 previously reported 5q- patients with adenomatous polyposis coli suggest that the gene responsible for GS/or familial polyposis coli (FPC) is in the 5q22 region, a result consistent with the findings of linkage 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