(Q52024867)
Statements
No apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndrome. (English)
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Chiurazzi P
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de Graaff E
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Ng J
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Verkerk AJ
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Wolfson S
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Fisch GS
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Kozak L
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Neri G
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Oostra BA
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1 July 1994
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51
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4
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309-314
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