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FMR1 gene mutations in patients with fragile X syndrome and obligate carriers: 30 years of experience in Chile.

Pubmed ID: 
27350105
Year: 
2016
Month: 
06
Volume: 
98
Citation: 
Santa María L, Aliaga S, Faundes V, Morales P, Pugin Á, Curotto B, Soto P, Peña MI, Salas I, Alliende MA. FMR1 gene mutations in patients with fragile X syndrome and obligate carriers: 30 years of experience in Chile. Genetics research 98 : e11(2016) PubMed