Items where authors include "Kernohan, KD"

Article

Bonnefoy, S, Watson, CM, Kernohan, KD et al. (22 more authors) (2018) Biallelic Mutations in LRRC56, Encoding a Protein Associated with Intraflagellar Transport, Cause Mucociliary Clearance and Laterality Defects. American Journal of Human Genetics, 103 (5). pp. 727-739. ISSN 0002-9297

Ito, Y, Carss, KJ, Duarte, ST et al. (18 more authors) (2018) De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures. American Journal of Human Genetics, 103 (1). pp. 144-153. ISSN 0002-9297

Conference or Workshop Item

Sheridan, EG orcid.org/0000-0002-7237-6280, Bonnefoy, S, Watson, CM et al. (17 more authors) (2019) Biallelic Mutations in LRRC56, encoding a protein associated with intraflagellar transport, causes defects in mucociliary clearance and laterality. In: 51st European Society of Human Genetics Conference, 16-19 Jun 2018, Milan, Italy.