Nuclear factors interact with a soybean beta-conglycinin enhancer.

por Allen, R D, Bernier, F, Lessard, P A, Beachy, R N
Publicado em 1989

Validation of an obstetric comorbidity index in an external population

por Metcalfe, A, Lix, LM, Johnson, J‐A, Currie, G, Lyon, AW, Bernier, F, Tough, SC
Publicado no BJOG (2015)

The value of mass screening for chlamydia control in high prevalence communities

por Hodgins, S, Peeling, R, Dery, S, Bernier, F, LaBrecque, A, Proulx, J, Joly, J, Alary, M, Mabey, D
Publicado em 2002

Diagnostic Performance of the Roche AMPLICOR PCR in Detecting Neisseria gonorrhoeae in Genitourinary Specimens from Female Sex Workers in Cotonou, Benin

por Mukenge-Tshibaka, L., Alary, M., Bernier, F., van Dyck, E., Lowndes, C. M., Guédou, A., Anagonou, S., Joly, J. R.
Publicado em 2000

Congenital hydrocephalus secondary to Walker-Warburg syndrome identified on the Manitoba Neonatal Screening Programme for Duchenne muscular dystrophy.

por Greenberg, C R, Jacobs, H K, Nylen, T E, Gibb, M, Chodirker, B N, Moffatt, M, Lacson, A, Halliday, W, Bernier, F, el-Husseini, A
Publicado em 1992

Sexually transmitted infections in male clients of female sex workers in Benin: risk factors and reassessment of the leucocyte esterase dipstick for screening of urethral infection...

por Alary, M, Lowndes, C, Mukenge-Tshibaka, L, Gnintoungbe, C, Bedard, E, Geraldo, N, Jossou, P, Lafia, E, Bernier, F, Baganizi, E, Joly, J, Frost, E, Anagonou, S
Publicado em 2003

MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement

por Donkervoort, S., Sabouny, R., Yun, P., Gauquelin, L., Chao, K. R., Hu, Y., Al Khatib, I., Töpf, A., Mohassel, P., Cummings, B. B., Kaur, R., Saade, D., Moore, S. A., Waddell, L. B., Farrar, M. A., Goodrich, J. K., Uapinyoying, P., Chan, S.H. S., Javed, A., Leach, M. E., Karachunski, P., Dalton, J., Medne, L., Harper, A., Thompson, C., Thiffault, I., Specht, S., Lamont, R. E., Saunders, C., Racher, H., Bernier, F. P., Mowat, D., Witting, N., Vissing, J., Hanson, R., Coffman, K. A., Hainlen, M., Parboosingh, J. S., Carnevale, A., Yoon, G., Schnur, R. E., Boycott, K. M., Mah, J. K., Straub, V., Foley, A. Reghan, Innes, A. M., Bönnemann, C. G., Shutt, T. E.
Publicado no Acta Neuropathol (2019)

Utility of whole‐exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care

por Sawyer, S.L., Hartley, T., Dyment, D.A., Beaulieu, C.L., Schwartzentruber, J., Smith, A., Bedford, H.M., Bernard, G., Bernier, F.P., Brais, B., Bulman, D.E., Warman Chardon, J., Chitayat, D., Deladoëy, J., Fernandez, B.A., Frosk, P., Geraghty, M.T., Gerull, B., Gibson, W., Gow, R.M., Graham, G.E., Green, J.S., Heon, E., Horvath, G., Innes, A.M., Jabado, N., Kim, R.H., Koenekoop, R.K., Khan, A., Lehmann, O.J., Mendoza‐Londono, R., Michaud, J.L., Nikkel, S.M., Penney, L.S., Polychronakos, C., Richer, J., Rouleau, G.A., Samuels, M.E., Siu, V.M., Suchowersky, O., Tarnopolsky, M.A., Yoon, G., Zahir, F.R., Majewski, J., Boycott, K.M.
Publicado no Clin Genet (2015)