Items where authors include "Berry, I"

Article

Lange, KI, Best, S, Tsiropoulou, S et al. (3 more authors) (2022) Interpreting ciliopathy-associated missense variants of uncertain significance (VUS) in Caenorhabditis elegans. Human Molecular Genetics, 31 (10). ddab344. pp. 1574-1587. ISSN 0964-6906

Stockdale, C, Rice, L, Carter, C et al. (7 more authors) (2021) Novel Case of Tripeptidyl Peptidase 2 Deficiency Associated with Mild Clinical Phenotype. Journal of Clinical Immunology, 41 (5). pp. 1123-1127. ISSN 0271-9142

Watson, CM orcid.org/0000-0003-2371-1844, Stockdale, C, Berry, I et al. (5 more authors) (2019) RNAseq Supports the Molecular Genetic Diagnosis of Late-Onset ADA Deficiency. Journal of Clinical Immunology, 39 (3). pp. 270-273. ISSN 0271-9142

Rice, L, Stockdale, C, Berry, I et al. (10 more authors) (2019) A Report of Novel STIM1 Deficiency and 6-Year Follow-Up of Two Previous Cases Associated with Mild Immunological Phenotype. Journal of Clinical Immunology, 39 (3). pp. 249-256. ISSN 0271-9142

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