Could a chimeric condition be responsible for unexpected genetic syndromes? The role of the single nucleotide polymorphism-array analysis.
Roberta BottegaStefania CappellaniAntonella FabrettoAlessandro Mauro SpinelliGiovanni Maria SeveriniMichelangelo AloisioMichela FaleschiniEmmanouil AthanasakisIrene BrunoFlavio FaletraVanna PecilePublished in: Molecular genetics & genomic medicine (2019)
In this paper, is reported the identification of two chimeric patients, a rare finding if sexual abnormalities are absent. However, their chimeric condition is responsible at least for the Silver-Russell phenotype observed in one of the two patients. By single nucleotide polymorphism-array analyses, it was possible to clearly define the mechanism responsible for this unusual finding, underlining the importance of this technique in bringing out the perhaps submerged world of chimeras.