Next generation sequencing reveals novel genetic variants (SRY, DMRT1, NR5A1, DHH, DHX37) in adults with 46,XY DSD von Buonocore, F, Clifford-Mobley, O, King, TFJ, Striglioni, N, Man, E, Suntharalingham, JP, del Valle, I, Lin, L, Lagos, CF, Rumsby, G, Conway, GS, Achermann, JC

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Predicted Benign and Synonymous Variants in CYP11A1 Cause Primary Adrenal Insufficiency Through Missplicing von Maharaj, A, Buonocore, F, Meimaridou, E, Ruiz-Babot, G, Guasti, L, Peng, H-M, Capper, CP, Burgos-Tirado, N, Prasad, R, Hughes, CR, Maudhoo, A, Crowne, E, Cheetham, TD, Brain, CE, Suntharalingham, JP, Striglioni, N, Yuksel, B, Gurbuz, F, Gupta, S, Lindsay, R, Couch, R, Spoudeas, HA, Guran, T, Johnson, S, Fowler, DJ, Conwell, LS, McInerney-Leo, AM, Drui, D, Cariou, B, Lopez-Siguero, JP, Harris, M, Duncan, EL, Hindmarsh, PC, Auchus, RJ, Donaldson, MD, Achermann, JC, Metherell, LA

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