Browsing by Author "Zahka, K"
Now showing items 1-2 of 2
Issue Date | Title | Author(s) |
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30 November 2021 | Elucidating the clinical spectrum and molecular basis of HYAL2 deficiency | Fasham, J; Lin, S; Ghosh, P; et al. |
12 January 2017 | Mutations 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. |