PubMed:31801603 / 326-622 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/31801603","sourcedb":"PubMed","sourceid":"31801603","source_url":"https://www.ncbi.nlm.nih.gov/pubmed/31801603","text":"We applied a combination of systematic experimental and bioinformatic methods to improve the molecular diagnosis of 39 patients with multiple congenital abnormalities and/or intellectual disability harboring apparent de novo SVs, most with an inconclusive diagnosis after regular genetic testing.","tracks":[{"project":"PubMed_Structured_Abstracts","denotations":[{"id":"T2","span":{"begin":0,"end":296},"obj":"METHODS"}],"attributes":[{"subj":"T2","pred":"source","obj":"PubMed_Structured_Abstracts"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"PubMed_Structured_Abstracts","color":"#b1ec93","default":true}]}]}}