Germline Activating JAK2 V617I Mutation, in a Family with Hereditary Thrombocytosis by Mead, A, Rugless, M, Woll, P, Clifford, R, Atkinson, D, Moule, S, Bienz, N, Wainscoat, J, Vyas, P, Henderson, S, Jacobsen, S, Schuh, A

Mutational analysis of the CDAN1 gene in familial and sporadic congenital dyserythropoietic anaemia type 1 by Ahmed, MR, Sternberg, A, Zahed, L, Taher, A, Haidar, J, Shamseddine, A, O'hea, A, Bienz, N, Dgany, O, Avidan, N, Beckmann, J, Tamary, H, Wood, W, Vyas, P, Wickramasinghe, S

In utero origin of myelofibrosis presenting in adult monozygotic twins by Sousos, N, Ní Leathlobhair, M, Simoglou Karali, C, Louka, E, Bienz, N, Royston, D, Clark, S-A, Hamblin, A, Howard, K, Mathews, V, George, B, Roy, A, Psaila, B, Wedge, DC, Mead, AJ

Germline activating JAK2-mutation in a family with hereditary thrombocytosis by Mead, A, Rugless, M, Woll, P, Clifford, R, Chowdhury, O, Dusa, A, Pecquet, C, Atkinson, D, Gatter, K, Moule, S, Bienz, N, Wainscoat, J, Vyas, P, Gale, R, Henderson, S, Constantinescu, S, Jacobsen, S, Schuh, A

Linkage and mutational analysis of the CDAN1 gene reveals genetic heterogeneity in congenital dyserythropoietic anemia type I. by Ahmed, MR, Chehal, A, Zahed, L, Taher, A, Haidar, J, Shamseddine, A, O'Hea, A, Bienz, N, Dgany, O, Avidan, N, Beckmann, J, Tamary, H, Higgs, D, Vyas, P, Wood, W, Wickramasinghe, SN

Impact of isolated germline JAK2V617I mutation on human hematopoiesis. by Mead, A, Chowdhury, O, Pecquet, C, Dusa, A, Woll, P, Atkinson, D, Burns, A, Score, J, Rugless, M, Clifford, R, Moule, S, Bienz, N, Vyas, P, Cross, N, Gale, R, Henderson, S, Constantinescu, SN, Schuh, A, Jacobsen, SE