UGT1A1 variation and gallstone formation in sickle cell disease. by Haverfield, E, McKenzie, C, Forrester, T, Bouzekri, N, Harding, R, Serjeant, G, Walker, T, Peto, T, Ward, R, Weatherall, D

Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen’s Inherited Cardiomyopathy Exp... by Kelly, M, Caleshu, C, Morales, A, Buchan, J, Wolf, Z, Harrison, S, Cook, S, Dillon, M, Garcia, J, Haverfield, E, Jongbloed, J, Macaya, D, Manrai, A, Orland, K, Richard, G, Spoonamore, K, Thomas, M, Thomson, K, Vincent, L, Walsh, R, Watkins, H, Whiffin, N, Ingles, J, Van Tintelen, J, Semsarian, C, Ware, J, Hershberger, R, Funke, B