Profiling Fragile X Syndrome in males: Strengths and weaknesses in cognitive abilities

Autor: G.J.A. Ramakers, B.J.C. Hamel, K.R. Ridderinkhof, Hilde M. Huizenga, Leopold M.G. Curfs, M.W. van der Molen, M.W. Van der Molen, Mariëtte Huizinga

Publikováno v: Research in Developmental Disabilities, 31, 2, pp. 426-39
Research in Developmental Disabilities, 31, 426-439. Elsevier B.V.
Research in Developmental Disabilities, 31, 426-39
Research in Developmental Disabilities, 31(2), 426-439. Elsevier
Research in Developmental Disabilities, 31(2), 426-439. Elsevier Inc.
Research in Developmental Disabilities, 31(2), 426-439. Elsevier Science
Van der Molen, M W J, Huizinga, M, Huizenga, H M, Ridderinkhof, K R, Hamel, B J C & Ramakers, G J A 2010, ' Profiling Fragile X Syndrome in Males: Strengths and weaknesses in cognitive abilities ', Research in Developmental Disabilities, vol. 31, no. 2, pp. 426-439 . https://doi.org/10.1016/j.ridd.2009.10.013

The present study examined the cognitive profile in Fragile X Syndrome (FXS) males, and investigated whether cognitive profiles are similar for FXS males at different levels of intellectual functioning. Cognitive abilities in non-verbal, verbal, memo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c064d44a863ab83215dec218b4d60e0
https://doi.org/10.1016/j.ridd.2009.10.013

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Tratamiento del síndrome del cromosoma X frágil desde la atención infantil temprana en España.

Autor: Robles-Bello, María Auxiliadora¹ auxiaziz@yahoo.es, Sánchez-Teruel, David¹

Publikováno v: Clinica y Salud. mar2013, Vol. 24 Issue 1, p19-26. 8p. 1 Chart, 1 Graph.

Founder Mutations in Inherited Cardiac Diseases in the Netherlands

Autor: Arthur A.M. Wilde, J. Peter van Tintelen

This booklet summarizes our current knowledge of founder mutation populations (‘extended families') in the Netherlands, among other aspects providing insight in where these patients can be expected (coloured maps of the prevalence in the 99 Dutch p