Items where authors include "Nampoothiri, S."

Article

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