APA

Chiurazzi P., de Graaff E., Ng J., Verkerk A. J., Wolfson S., Fisch G. S., Kozak L., Neri G. & Oostra B. A. (19941116). No apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndrome. : American journal of medical genetics.

Chicago

Chiurazzi P, de Graaff E, Ng J, Verkerk A J, Wolfson S, Fisch G S, Kozak L, Neri G and Oostra B A. 19941116. No apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndrome. : American journal of medical genetics.

Harvard

Chiurazzi P., de Graaff E., Ng J., Verkerk A. J., Wolfson S., Fisch G. S., Kozak L., Neri G. and Oostra B. A. (19941116). No apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndrome. : American journal of medical genetics.

MLA

Chiurazzi P, de Graaff E, Ng J, Verkerk A J, Wolfson S, Fisch G S, Kozak L, Neri G and Oostra B A. No apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndrome. : American journal of medical genetics. 19941116.