Predictive DNA testing in ophthalmology: View 1

af Héon, E
Udgivet 2003

Outer retinal structural anomaly due to frameshift mutation in CACNA1F gene

af Vincent, A, Héon, E
Udgivet 2012

Predictive DNA testing in ophthalmology

af Mackey, D A, Héon, E, Webster, A R
Udgivet 2003

Retinal microstructure in patients with EFEMP1 retinal dystrophy evaluated by Fourier domain OCT

af Gerth, C, Zawadzki, RJ, Werner, JS, Héon, E
Udgivet 2008

BEST1-related autosomal dominant vitreoretinochoroidopathy: a degenerative disease with a range of developmental ocular anomalies

af Vincent, A, McAlister, C, VandenHoven, C, Héon, E
Udgivet 2011

Molecular characterisation of congenital glaucoma in a consanguineous Canadian community: a step towards preventing glaucoma related blindness

af Martin, S, Sutherland, J., Levin, A., Klose, R., Priston, M., Heon, E.
Udgivet 2000

A microstructural retinal analysis of membrano-proliferative glomerulonephritis type II

af Gerth, C, Zawadzki, R J, Licht, C, Werner, J S, Héon, E
Udgivet 2008

Enhanced Foamability with Shrinking Microfibers in Linear Polymer

af Kim, Eric S., Park, Heon E., Lopez-Barron, Carlos R., Lee, Patrick C.
Udgivet i Polymers (Basel) (2019)

Specific retinal phenotype in early IQCB1-related disease

af Vincent, A, AlAli, A, MacDonald, H, VandenHoven, C, Héon, E
Udgivet i Eye (Lond) (2018)

A novel GJA8 mutation in an Iranian family with progressive autosomal dominant congenital nuclear cataract

af Willoughby, C, Arab, S., Gandhi, R, Zeinali, S, Arab, S., Luk, D, Billingsley, G, Munier, F, Heon, E
Udgivet 2003

Ultrasound biomicroscopy in the management of retinoblastoma

af Vasquez, L M, Giuliari, G P, Halliday, W, Pavlin, C J, Gallie, B L, Héon, E
Udgivet 2011

Gene localization for aculeiform cataract, on chromosome 2q33-35.

af Héon, E, Liu, S, Billingsley, G, Bernasconi, O, Tsilfidis, C, Schorderet, D F, Munier, F L, Tsifildis, C
Udgivet 1998

A common gene for juvenile and adult-onset primary open-angle glaucomas confined on chromosome 1q.

af Morissette, J, Côté, G, Anctil, J L, Plante, M, Amyot, M, Héon, E, Trope, G E, Weissenbach, J, Raymond, V
Udgivet 1995

Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly

af Vincent, A., Billingsley, G., Priston, M., Williams-Lyn, D., Sutherland, J., Glaser, T., Oliver, E., Walter, M., Heathcote, G., Levin, A., Heon, E.
Udgivet 2001

Porcine Lung-Derived Extracellular Matrix Hydrogel Properties Are Dependent on Pepsin Digestion Time

af Pouliot, Robert A., Young, Bethany M., Link, Patrick A., Park, Heon E., Kahn, Alison R., Shankar, Keerthana, Schneck, Matthew B., Weiss, Daniel J., Heise, Rebecca L.
Udgivet i Tissue Eng Part C Methods (2020)

Avian lungs: A novel scaffold for lung bioengineering

af Wrenn, Sean M., Griswold, Ethan D., Uhl, Franziska E., Uriarte, Juan J., Park, Heon E., Coffey, Amy L., Dearborn, Jacob S., Ahlers, Bethany A., Deng, Bin, Lam, Ying-Wai, Huston, Dryver R., Lee, Patrick C., Wagner, Darcy E., Weiss, Daniel J.
Udgivet i PLoS One (2018)

Mutation analysis of patients with Hermansky-Pudlak syndrome: a frameshift hot spot in the HPS gene and apparent locus heterogeneity.

af Oh, J, Ho, L, Ala-Mello, S, Amato, D, Armstrong, L, Bellucci, S, Carakushansky, G, Ellis, J P, Fong, C T, Green, J S, Heon, E, Legius, E, Levin, A V, Nieuwenhuis, H K, Pinckers, A, Tamura, N, Whiteford, M L, Yamasaki, H, Spritz, R A
Udgivet 1998

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

af 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.
Udgivet i Clin Genet (2015)