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Seri M, Cusano R, Gangarossa S, Caridi G, Bordo D, Lo Nigro C, Ghiggeri GM, Ravazzolo R, Savino M, Del Vecchio M, d'Apolito M, Iolascon A, Zelante LL, Savoia A, Balduini CL, Noris P, Magrini U, Belletti S, Heath KE, Babcock M, Glucksman MJ, Aliprandis E, Bizzaro N, Desnick RJ, Martignetti JA. Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium. Nat Genet 2000; 26: 103-5.
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Seri, M.1
Cusano, R.2
Gangarossa, S.3
Caridi, G.4
Bordo, D.5
Lo Nigro, C.6
Ghiggeri, G.M.7
Ravazzolo, R.8
Savino, M.9
Del Vecchio, M.10
D'Apolito, M.11
Iolascon, A.12
Zelante, L.L.13
Savoia, A.14
Balduini, C.L.15
Noris, P.16
Magrini, U.17
Belletti, S.18
Heath, K.E.19
Babcock, M.20
Glucksman, M.J.21
Aliprandis, E.22
Bizzaro, N.23
Desnick, R.J.24
Martignetti, J.A.25
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Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly
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Kelley MJ, Jawien W, Ortel TL, Korczak JF. Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly. Nat Genet 2000; 26: 106-8.
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Kelley, M.J.1
Jawien, W.2
Ortel, T.L.3
Korczak, J.F.4
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