Now showing items 1-2 of 2

    Issue DateTitleAuthor(s)
    21 October 2021Obesity-associated GNAS mutations and the melanocortin pathway.  Mendes de Oliveira, E; Keogh, JM; Talbot, F; et al.
    6 February 2020Using referral rates for genetic testing to determine the incidence of a rare disease: The minimal incidence of congenital hyperinsulinism in the UK is 1 in 28,389  Yau, D; Laver, TW; Dastamani, A; et al.