Publications

Export 2 results:
Author Title [ Year(Asc)]
Filters: Author is Wolf, Whitney E  [Clear All Filters]
2019
Hannah, W. B. et al. The expanding phenotype of OFD1-related disorders: Hemizygous loss-of-function variants in three patients with primary ciliary dyskinesia. Mol Genet Genomic Med 7, e911 (2019).
2014
Knowles, M. R. et al. Mutations in RSPH1 cause primary ciliary dyskinesia with a unique clinical and ciliary phenotype. Am J Respir Crit Care Med 189, 707-17 (2014).