Ullman MT, Pierpont EI (June 2005). "Specific language impairment is not specific to language: the procedural deficit hypothesis". Cortex; A Journal Devoted to the Study of the Nervous System and Behavior. 41 (3): 399–433. doi:10.1016/s0010-9452(08)70276-4. PMID15871604. S2CID1027740.
Knecht S, Deppe M, Dräger B, Bobe L, Lohmann H, Ringelstein E, etal. (January 2000). "Language lateralization in healthy right-handers". Brain. 123 (1): 74–81. doi:10.1093/brain/123.1.74. PMID10611122.
Pujol J, Deus J, Losilla JM, Capdevila A (March 1999). "Cerebral lateralization of language in normal left-handed people studied by functional MRI". Neurology. 52 (5): 1038–1043. doi:10.1212/WNL.52.5.1038. PMID10102425. S2CID45298083.
Hurst JA, Baraitser M, Auger E, Graham F, Norell S (April 1990). "An extended family with a dominantly inherited speech disorder". Developmental Medicine and Child Neurology. 32 (4): 352–355. doi:10.1111/j.1469-8749.1990.tb16948.x. PMID2332125. S2CID2654363.
Vargha-Khadem F, Gadian DG, Copp A, Mishkin M (February 2005). "FOXP2 and the neuroanatomy of speech and language". Nature Reviews. Neuroscience. 6 (2): 131–138. doi:10.1038/nrn1605. PMID15685218. S2CID2504002.
Liégeois F, Baldeweg T, Connelly A, Gadian DG, Mishkin M, Vargha-Khadem F (November 2003). "Language fMRI abnormalities associated with FOXP2 gene mutation". Nature Neuroscience. 6 (11): 1230–1237. doi:10.1038/nn1138. PMID14555953. S2CID31003547.
Gauger LM, Lombardino LJ, Leonard CM (December 1997). "Brain morphology in children with specific language impairment". Journal of Speech, Language, and Hearing Research. 40 (6): 1272–1284. doi:10.1044/jslhr.4006.1272. PMID9430748.
Webster RI, Erdos C, Evans K, Majnemer A, Saigal G, Kehayia E, etal. (August 2008). "Neurological and magnetic resonance imaging findings in children with developmental language impairment". Journal of Child Neurology. 23 (8): 870–877. doi:10.1177/0883073808315620. PMID18660471. S2CID206547104.
Ullman MT, Pierpont EI (June 2005). "Specific language impairment is not specific to language: the procedural deficit hypothesis". Cortex; A Journal Devoted to the Study of the Nervous System and Behavior. 41 (3): 399–433. doi:10.1016/s0010-9452(08)70276-4. PMID15871604. S2CID1027740.
Knecht S, Deppe M, Dräger B, Bobe L, Lohmann H, Ringelstein E, etal. (January 2000). "Language lateralization in healthy right-handers". Brain. 123 (1): 74–81. doi:10.1093/brain/123.1.74. PMID10611122.
Pujol J, Deus J, Losilla JM, Capdevila A (March 1999). "Cerebral lateralization of language in normal left-handed people studied by functional MRI". Neurology. 52 (5): 1038–1043. doi:10.1212/WNL.52.5.1038. PMID10102425. S2CID45298083.
Hurst JA, Baraitser M, Auger E, Graham F, Norell S (April 1990). "An extended family with a dominantly inherited speech disorder". Developmental Medicine and Child Neurology. 32 (4): 352–355. doi:10.1111/j.1469-8749.1990.tb16948.x. PMID2332125. S2CID2654363.
Vargha-Khadem F, Gadian DG, Copp A, Mishkin M (February 2005). "FOXP2 and the neuroanatomy of speech and language". Nature Reviews. Neuroscience. 6 (2): 131–138. doi:10.1038/nrn1605. PMID15685218. S2CID2504002.
Liégeois F, Baldeweg T, Connelly A, Gadian DG, Mishkin M, Vargha-Khadem F (November 2003). "Language fMRI abnormalities associated with FOXP2 gene mutation". Nature Neuroscience. 6 (11): 1230–1237. doi:10.1038/nn1138. PMID14555953. S2CID31003547.
Gauger LM, Lombardino LJ, Leonard CM (December 1997). "Brain morphology in children with specific language impairment". Journal of Speech, Language, and Hearing Research. 40 (6): 1272–1284. doi:10.1044/jslhr.4006.1272. PMID9430748.
Webster RI, Erdos C, Evans K, Majnemer A, Saigal G, Kehayia E, etal. (August 2008). "Neurological and magnetic resonance imaging findings in children with developmental language impairment". Journal of Child Neurology. 23 (8): 870–877. doi:10.1177/0883073808315620. PMID18660471. S2CID206547104.
Ullman MT, Pierpont EI (June 2005). "Specific language impairment is not specific to language: the procedural deficit hypothesis". Cortex; A Journal Devoted to the Study of the Nervous System and Behavior. 41 (3): 399–433. doi:10.1016/s0010-9452(08)70276-4. PMID15871604. S2CID1027740.
Pujol J, Deus J, Losilla JM, Capdevila A (March 1999). "Cerebral lateralization of language in normal left-handed people studied by functional MRI". Neurology. 52 (5): 1038–1043. doi:10.1212/WNL.52.5.1038. PMID10102425. S2CID45298083.
Hurst JA, Baraitser M, Auger E, Graham F, Norell S (April 1990). "An extended family with a dominantly inherited speech disorder". Developmental Medicine and Child Neurology. 32 (4): 352–355. doi:10.1111/j.1469-8749.1990.tb16948.x. PMID2332125. S2CID2654363.
Vargha-Khadem F, Gadian DG, Copp A, Mishkin M (February 2005). "FOXP2 and the neuroanatomy of speech and language". Nature Reviews. Neuroscience. 6 (2): 131–138. doi:10.1038/nrn1605. PMID15685218. S2CID2504002.
Liégeois F, Baldeweg T, Connelly A, Gadian DG, Mishkin M, Vargha-Khadem F (November 2003). "Language fMRI abnormalities associated with FOXP2 gene mutation". Nature Neuroscience. 6 (11): 1230–1237. doi:10.1038/nn1138. PMID14555953. S2CID31003547.
Webster RI, Erdos C, Evans K, Majnemer A, Saigal G, Kehayia E, etal. (August 2008). "Neurological and magnetic resonance imaging findings in children with developmental language impairment". Journal of Child Neurology. 23 (8): 870–877. doi:10.1177/0883073808315620. PMID18660471. S2CID206547104.
Hans Van Balkom, Verhoeven, Ludo Th (2004). Classification of developmental language disorders: theoretical issues and clinical implications. Hillsdale, N.J: Lawrence Erlbaum Associates. ISBN978-0-8058-4122-0. OCLC803128031.