Sybert, Virginia P.

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

Postnatal outcomes of prenatally diagnosed 45,X/46,XX

Tokita, M. J., & Sybert, V. P. (2016) · American Journal of Medical Genetics Part A

Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesPrenatal Screening and Diagnostics

Cited by 58

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

Cardiovascular outcomes of pregnancy in Turner syndrome

Grewal, J., Valente, A. M., Egbe, A. C., Wu, F. M., Krieger, E. V., Sybert, V. P., van Hagen, I. M., Beauchesne, L. M., Rodriguez, F. H., Broberg, C. S., et al. (2021) · Heart

Cardiovascular Issues in PregnancyCongenital Heart Disease Studies

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