论文信息 - A novel FMR1 PCR method for the routine detection of low abundance expanded alleles and full mutations in fragile X syndrome. - 字舞流文

A novel FMR1 PCR method for the routine detection of low abundance expanded alleles and full mutations in fragile X syndrome.

E. Sekinger | P. Hagerman | F. Tassone | Sachin Sah | A. Hadd | Liangjing Chen | Julie Krosting | G. Latham | T. Stenzel | S. Filipovic-Sadic | Wenting Zhang