PMC:1852721 / 49778-50252 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PMC/sourceid/1852721","sourcedb":"PMC","sourceid":"1852721","source_url":"https://www.ncbi.nlm.nih.gov/pmc/1852721","text":"Inversions can also cause birth defects or neoplasia, either by gene disruption produced by the break at one end or by the bringing together of control elements of one gene with the coding portion of another. An inversion in the long arm of chromosome 2 was a clue to the location of the gene for Waardenburg syndrome type 1. Inversions and other aberrations involving 16p were the only evidence of the location of the gene mutant in Rubinstein-Taybi syndrome (MIM #180849).","tracks":[]}