Nuclear factors interact with a soybean beta-conglycinin enhancer.

le Allen, R D, Bernier, F, Lessard, P A, Beachy, R N
Foilsithe 1989

Validation of an obstetric comorbidity index in an external population

le Metcalfe, A, Lix, LM, Johnson, J‐A, Currie, G, Lyon, AW, Bernier, F, Tough, SC
Foilsithe in BJOG (2015)

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

le Hodgins, S, Peeling, R, Dery, S, Bernier, F, LaBrecque, A, Proulx, J, Joly, J, Alary, M, Mabey, D
Foilsithe 2002

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

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

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

le 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
Foilsithe 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...

le 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
Foilsithe 2003

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

le 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.
Foilsithe in Acta Neuropathol (2019)

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

le 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.
Foilsithe in Clin Genet (2015)