Wohlfart, Sigrun

Prenatal correction of x-linked hypohidrotic ectodermal dysplasia

Schneider, H., Faschingbauer, F., Schuepbach-Mallepell, S., Körber, I., Wohlfart, S., Dick, A., Wahlbuhl, M., Kowalczyk-Quintas, C., Vigolo, M., Kirby, N., et al. (2018) · New England Journal of Medicine

dental development and anomaliesGenetic and rare skin diseases.

Cited by 183

Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements

Wohlfart, S., Hammersen, J., & Schneider, H. (2016) · Journal of Human Genetics

dental development and anomaliesGenetic and rare skin diseases.

Cited by 41

Sweating ability of patients with p63-associated syndromes

Ferstl, P., Wohlfart, S., & Schneider, H. (2018) · European Journal of Pediatrics

Genetic and rare skin diseases.dental development and anomalies

Cited by 8