APA

Tzountzouris J., Kennedy D., Skuterud M., Connolly-Wilson M., Holden J. J., Lin C. C., Mak-Tam E., Somerville M. J., Summers A. M. & Allingham-Hawkins D. J. (20010201). Apparently unstable normal FMR1 alleles in nine developmentally delayed patients: implications for molecular diagnosis of the fragile X syndrome. : Genetic testing.

Chicago

Tzountzouris J, Kennedy D, Skuterud M, Connolly-Wilson M, Holden J J, Lin C C, Mak-Tam E, Somerville M J, Summers A M and Allingham-Hawkins D J. 20010201. Apparently unstable normal FMR1 alleles in nine developmentally delayed patients: implications for molecular diagnosis of the fragile X syndrome. : Genetic testing.

Harvard

Tzountzouris J., Kennedy D., Skuterud M., Connolly-Wilson M., Holden J. J., Lin C. C., Mak-Tam E., Somerville M. J., Summers A. M. and Allingham-Hawkins D. J. (20010201). Apparently unstable normal FMR1 alleles in nine developmentally delayed patients: implications for molecular diagnosis of the fragile X syndrome. : Genetic testing.

MLA

Tzountzouris J, Kennedy D, Skuterud M, Connolly-Wilson M, Holden J J, Lin C C, Mak-Tam E, Somerville M J, Summers A M and Allingham-Hawkins D J. Apparently unstable normal FMR1 alleles in nine developmentally delayed patients: implications for molecular diagnosis of the fragile X syndrome. : Genetic testing. 20010201.