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5. Verkerk, A.J.M.H.; Pieretti, M.; Sutcliffe, J.S.; Fu, Y.-H.; Kuhl, D.P.A.; Pizzuti, A.; Reiner, O.; Richards, S.; Victoria, M.F.; Zhang, F.; Eussen, B.E.; van Ommen, G.-J.B.; Blonden, L.A.J.; Riggins, G.J.; Chastain, J.L.; Kunst, C.B.; Galjaard, H.; Caskey, C.T.; Nelson, D.L.; Oostra, B.A.; Warren, S.T. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell 1991, 65, 905-914.

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14. Fu, Y.-H.; Kuhl, D.P.A.; Pizzuti, A.; Pieretti, M.; Sutcliffe, J.S.; Richards, S.; Verkerk, A.J.M.H.; Holden, J.J.A.; Fenwick, R.G., Jr.; Warren, S.T.; Oostra, B.A.; Nelson, D.L.; Caskey, C.T. Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox. Cell 1991, 67, 10471058.

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W.T. Detection of full fragile X mutation. Lancet 1992, 339, 271-272.

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B.B.A.; Hilhorst-Hofstee, Y.; Smits, A.; van Looveren, E.; Willems, P.J.; Galjaard, H.; Oostra, B.A. Noninvasive test for fragile X syndrome, using hair root analysis. Am. J. Hum. Genet. 1999, 65, 98-103.

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Gaucher Disease

100 Pregnancy Tips

100 Pregnancy Tips

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