Now showing items 1-2 of 2

    Issue DateTitleAuthor(s)
    30 November 2021Elucidating the clinical spectrum and molecular basis of HYAL2 deficiency  Fasham, J; Lin, S; Ghosh, P; et al.
    12 January 2017Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndrome of Orofacial Clefting and Cor Triatriatum Sinister in Humans and Mice.  Muggenthaler, MMA; Chowdhury, B; Hasan, SN; et al.