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All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year Sort by creator [A → Z]' creator [Z → A]' publishing year ↑ (asc)' publishing year ↓ (desc)' title [A → Z]' title [Z → A]' Simple Search Hits 1 – 12 of 12 1 Bang for your buck: CAS tx amount distribution (Maas et al., 2019) ... Maas, Edwin; Gildersleeve-Neumann, Christina; Jakielski, Kathy. - : ASHA journals, 2019 BASE Show details 2 Bang for your buck: CAS tx amount distribution (Maas et al., 2019) ... Maas, Edwin; Gildersleeve-Neumann, Christina; Jakielski, Kathy. - : ASHA journals, 2019 BASE Show details 3 Estimates of the prevalence of speech and motor speech disorders in persons with complex neurodevelopmental disorders ... Shriberg, Lawrence D.; Strand, Edythe A.; Jakielski, Kathy J.. - : Taylor & Francis, 2019 BASE Show details 4 Estimates of the prevalence of speech and motor speech disorders in persons with complex neurodevelopmental disorders ... Shriberg, Lawrence D.; Strand, Edythe A.; Jakielski, Kathy J.. - : Taylor & Francis, 2019 BASE Show details 5 Estimates of the prevalence of speech and motor speech disorders in persons with complex neurodevelopmental disorders ... Shriberg, Lawrence D.; Strand, Edythe A.; Jakielski, Kathy J.. - : Taylor & Francis, 2019 BASE Show details 6 Estimates of the prevalence of speech and motor speech disorders in persons with complex neurodevelopmental disorders Shriberg, Lawrence D.; Strand, Edythe A.; Jakielski, Kathy J.. - 2019 BASE Show details 7 A set of regulatory genes co-expressed in embryonic human brain is implicated in disrupted speech development Eising, Else; Carrion-Castillo, Amaia; Vino, Arianna... In: ISSN: 1359-4184 ; EISSN: 1476-5578 ; Molecular Psychiatry ; https://hal.archives-ouvertes.fr/hal-01726218 ; Molecular Psychiatry, Nature Publishing Group, In press (2018) BASE Show details 8 CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language Snijders Blok, Lot; Rousseau, Justine; Twist, Joanna... In: ISSN: 2041-1723 ; EISSN: 2041-1723 ; Nature Communications ; https://hal.sorbonne-universite.fr/hal-01922858 ; Nature Communications, Nature Publishing Group, 2018, 9 (1), pp.4619. ⟨10.1038/s41467-018-06014-6⟩ (2018) BASE Show details 9 Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome Raca, Gordana; Baas, Becky S; Kirmani, Salman. - : Nature Publishing Group, 2013 BASE Show details 10 Encoding, memory, and transcoding deficits in childhood apraxia of speech Strand, Edythe A.; Jakielski, Kathy J.; Lohmeier, Heather L.... In: Clinical linguistics & phonetics. - London : Informa Healthcare 26 (2012) 5, 445-482 BLLDB OLC Linguistik Show details 11 Phenotype of FOXP2 Haploinsufficiency in a Mother and Son Rice, Gregory M.; Raca, Gordana; Jakielski, Kathy J.. - 2011 BASE Show details 12 Developmental apraxia of speech : determiners of differential diagnosis Davis, Barbara L.; Jakielski, Kathy J.; Marquardt, Thomas P. In: Clinical linguistics & phonetics. - London : Informa Healthcare 12 (1998) 1, 25-45 BLLDB Show details

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