Browse by Person

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | No Grouping
Jump to: Article
Number of items: 2.


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

Robson, EA, Chetcuti, P, Hirst, RA et al. (6 more authors) (2017) Update on primary ciliary dyskinesia. Paediatrics and Child Health, 27 (7). pp. 337-342. ISSN 1751-7222

This list was generated on Mon Jan 20 05:52:48 2020 GMT.