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Absence of the fragile X CGG trinucleotide repeat expansion in girls diagnosed with a pervasive developmental disorder
Gretchen A. Meyer, Nathan J. Blum, Wendy Hitchcock, Paolo FortinaVolume:
133
Year:
1998
Language:
english
DOI:
10.1016/s0022-3476(98)70270-7
File:
PDF, 28 KB
english, 1998