Items where authors include "Majethia, P."

Article

Godfrey, M. orcid.org/0000-0002-1636-3434, Levy, M.A., Campbell, C. et al. (38 more authors) (2026) An episignature informed systematic analysis to ascertain the clinical significance and consequences of CHD8 missense variants. European Journal of Human Genetics. ISSN 1018-4813

Chaurasia, A., Shukla, A., Pande, S. et al. (23 more authors) (2026) Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disorders. European Journal of Human Genetics, 34. pp. 1059-1069. ISSN 1018-4813