A systematic mutation screening approach for syndromic and nonsyndromic forms of mental retardation in human Xp21.1-Xp11.23

J Ramser,G Wen, IM Garay, M Dufault,H Hellebrand,S Engert,C Schwartz,M Platzer, A Meindl

EUROPEAN JOURNAL OF HUMAN GENETICS(2002)

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