Publications
Export 2 results:
Author Title [ Year] Filters: Keyword is Female and Author is Roosing, Susanne [Clear All Filters]
Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar Hypoplasia. Am J Hum Genet 101, 441-450 (2017).
Mutations in CEP120 cause Joubert syndrome as well as complex ciliopathy phenotypes. J Med Genet 53, 608-15 (2016).