Search Results - Hetalkumar Panchal

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    Novel variant in NSDHL gene associated with CHILD syndrome and syndactyly- a case report by D. Hettiarachchi, Hetalkumar Panchal, P. S. Lai, V. H. W. Dissanayake

    Published 2020
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    Novel frameshift variant in the PCNT gene associated with Microcephalic Osteodysplastic Primordial Dwarfism (MOPD) Type II and small kidneys by D. Hettiarachchi, S. M. V. Subasinghe, G. G. Anandagoda, Hetalkumar Panchal, P. S. Lai, V. H. W. Dissanayake

    Published 2022
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