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Publisher: Wiley-Blackwell

Volume 51, Number 5, May 2007

Deletions of VCX-A and NLGN4: a variable phenotype including normal intellect
pp. 329-333(5)
Authors: Macarov, M.; Zeigler, M.; Newman, J. P.; Strich, D.; Sury, V.; Tennenbaum, A.; Meiner, V.

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A neuropsychological assessment of frontal cognitive functions in Prader–Willi syndrome
pp. 350-365(16)
Authors: Jauregi, J.; Arias, C.; Vegas, O.; Alén, F.; Martinez, S.; Copet, P.; Thuilleaux, D.

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Gender differences in repetitive language in fragile X syndrome
pp. 387-400(14)
Authors: Murphy, M. M.; Abbeduto, L.

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Specific language impairment as the prominent feature in a patient with a low-level trisomy 21 mosaicism
pp. 401-405(5)
Authors: Paoloni-Giacobino, A.; Lemieux, N.; Lemyre, E.; Lespinasse, J.

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