Report of a patient with fragile X syndrome unexpectedly identified by karyotype analysis
Maiara A. Floriani; Marcelo R. Vilas Boas; Rafael Fabiano M. Rosa; Patrícia Trevisan; Luiza Emy Dorfman; Rosana C. M. Rosa; Tatiana D. Zen; Paulo Ricardo G. ZenJ. Bras. Patol. Med. Lab. 2017;53(2):108-109DOI: 10.5935/1676-2444.20170017 ABSTRACT Fragile X syndrome is considered the main known cause of inherited learning disabilities and it is characterized by mutations in the FMR1 gene. […]