Fete, Mary

Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway.

Wright, J. T., Fete, M., Schneider, H., Zinser, M., Koster, M. I., Clarke, A. J., Hadj‐Rabia, S., Tadini, G., Pagnan, N., Visinoni, A. F., et al. (2019) · American Journal of Medical Genetics Part A

dental development and anomaliesGenetic and rare skin diseases.

Cited by 185

Molecular Pathway-Based Classification of Ectodermal Dysplasias: First Five-Yearly Update

Peschel, N., Wright, J. T., Koster, M. I., Clarke, A. J., Tadini, G., Fete, M., Hadj-Rabia, S., Sybert, V. P., Norderyd, J., Maier-Wohlfart, S., et al. (2022) · Genes

dental development and anomaliesGenetic and rare skin diseases.

Cited by 60

International research symposium on ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome

Fete, M., vanBokhoven, H., Clements, S. E., McKeon, F., Roop, D. R., Koster, M. I., Missero, C., Attardi, L. D., Lombillo, V. A., Ratovitski, E., et al. (2009) · American Journal of Medical Genetics Part A

Genetic and rare skin diseases.dental development and anomalies

Cited by 40

Prevalence of atopic disorders and immunodeficiency in patients with ectodermal dysplasia syndromes

Mark, B. J., Becker, B. A., Halloran, D. R., Bree, A. F., Sindwani, R., Fete, M. D., Motil, K. J., Srun, S. W., & Fete, T. J. (2012) · Annals of Allergy, Asthma & Immunology

dental development and anomaliesImmunodeficiency and Autoimmune Disorders

Cited by 38