Linguistic and psychomotor development in children with chromosome 14 deletions

References

• Åkefeldt, A., Åkefeldt, B., & Gillberg, C. (1997). Voice, speech and language characteristics of children with Prader–Willi syndrome. Journal of Intellectual Disability Research, 41(4), 302–311.
   PubMed Web of Science ®Google Scholar
• Atkin, K., & Lorch M. P. (2007). Language development in a 3-year-old boy with Prader–Willi syndrome. Clinical Linguistics & Phonetics, 21(4), 261–276.
   PubMed Web of Science ®Google Scholar
• Baird, G., Charman, T., Pickles, A., Chandler, S., Loucas, T., Meldrum, D., Carcani-Rathwell, I., Serkana D, & Simonoff, E. (2008). Regression, developmental trajectory and associated problems in disorders in the autism spectrum: The SNAP study. Journal of Autism and Developmental Disorders, 38, 1827–1836.
   PubMed Web of Science ®Google Scholar
• Caselli, M. C., & Casadio, P. (1995). Il Primo Vocabolario del Bambino [Children's First Words]. Milan: Franco Angeli.
   Google Scholar
• Charman, T., Taylor, E., Drew, A., Cockerill, H., Brown, J. A., & Baird, G. (2005). Outcome at 7 years of children diagnosed with autism at age 2: Predictive validity of assessments conducted at 2 and 3 years of age and pattern of symptom change over time. Journal of Child Psychology and Psychiatry, 46(5), 500–513.
   PubMed Web of Science ®Google Scholar
• D'Odorico, L., Giovannini, S., Majorano, M., Martinelli, P. & Zampini, L. (2011). Competenze linguistiche in bambini di lingua italiana con aberrazioni del cromosoma 14 [Linguistic skills in Italian children with chromosome 14 aberrations]. Psichiatria dell'Infanzia e dell'Adolescenza, 78(2), 449–456.
   Google Scholar
• D'Odorico, L., & Jacob, V. (2006). Prosodic and lexical aspects of maternal linguistic input to late-talking toddlers. International Journal of Language & Communication Disorders, 41, 293–311.
   PubMed Web of Science ®Google Scholar
• Dressler, A., Perelli, V., Bozza, M., & Bargagna, S. (2011). The autistic phenotype in Down syndrome: Differences in adaptive behaviour versus Down syndrome alone and autistic disorder alone. Functional Neurology, 26(3), 151–158.
   PubMed Web of Science ®Google Scholar
• Kristoffersen, K. E. (2008). Consonants in Cri du chat syndrome: A case study. Journal of Communication Disorders, 41, 179–202.
   PubMed Web of Science ®Google Scholar
• Kristoffersen, K. E. (2012). Inflectional morphology in cri du chat syndrome. A case study. Clinical Linguistics & Phonetics, 26(2), 120–134.
   PubMed Web of Science ®Google Scholar
• Lord, C., Rutter, M., Di Lavore, P. C., & Risi, S. (1999). Autism Diagnostic Observation Schedule – WPS (ADOS-WPS). Los Angeles, CA: Western Psychological Services.
   Google Scholar
• Luiz, D., Barnard, A., Knoesen, N., Kotras, N., Horrocks, S., McAlinden, P., Challis, D., & O'Connell, R. (2006). GMDS-ER 2–8 – Griffiths Mental Development Scales –Extended Revised: 2 to 8 years. Italian edition edited by C. Cianchetti, & G. S. Fancello (Eds.). Firenze: Giunti Organizzazioni Speciali.
   Google Scholar
• MacWhinney, B. (2000). The CHILDES Project: Tools for analyzing talk, 3rd edn. Mahwah, NJ: Lawrence Erlbaum Associates.
   Google Scholar
• Van Karnebeek, C. D. M., Quik, S., Sluijeter, S., Hulsbeek, M. M. F., Hoovers, J. M. N., & Hennekam, R. C. M. (2002). Further delineation of the chromosome 14q terminal deletion syndrome. American Journal of Medical Genetics, 110, 65–72.
   PubMed Web of Science ®Google Scholar
• Zampini, L., & D'Odorico, L. (2011a). Gesture production and language development: a longitudinal study of children with Down syndrome. Gesture, 11(2), 174–193.
   Web of Science ®Google Scholar
• Zampini, L., & D'Odorico, L. (2011b). Lexical and syntactic development in Italian children with Down syndrome. International Journal of Language & Communication Disorders, 46(4), 386–396.
   PubMed Web of Science ®Google Scholar
• Zollino, M., Ponzi, E., Gobbi, G., & Neri, G. (2012). The ring 14 syndrome. European Journal of Medical Genetics, 55, 374–380.
   PubMed Web of Science ®Google Scholar
• Zollino, M., Seminara, L., Orteschi, D., Gobbi, G., Giovannini, S., Della Giustina, E., Frattini, D., Scarano, A., & Neri G. (2009). The ring14 syndrome: Clinical and molecular definition. American Journal of Medical Genetics, 6, 1116–1124.
   Web of Science ®Google Scholar