APA

Neerman-Arbez M., de Moerloose P., Honsberger A., Parlier G., Arnuti B., Biron C., Borg J. Y., Eber S., Meili E., Peter-Salonen K., Ripoll L., Vervel C., d'Oiron R., Staeger P., Antonarakis S. E. & Morris M. A. (20010531). Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes. : Human genetics.

Chicago

Neerman-Arbez M, de Moerloose P, Honsberger A, Parlier G, Arnuti B, Biron C, Borg J Y, Eber S, Meili E, Peter-Salonen K, Ripoll L, Vervel C, d'Oiron R, Staeger P, Antonarakis S E and Morris M A. 20010531. Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes. : Human genetics.

Harvard

Neerman-Arbez M., de Moerloose P., Honsberger A., Parlier G., Arnuti B., Biron C., Borg J. Y., Eber S., Meili E., Peter-Salonen K., Ripoll L., Vervel C., d'Oiron R., Staeger P., Antonarakis S. E. and Morris M. A. (20010531). Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes. : Human genetics.

MLA

Neerman-Arbez M, de Moerloose P, Honsberger A, Parlier G, Arnuti B, Biron C, Borg J Y, Eber S, Meili E, Peter-Salonen K, Ripoll L, Vervel C, d'Oiron R, Staeger P, Antonarakis S E and Morris M A. Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes. : Human genetics. 20010531.