Found: 7
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Delving into the Genetic Causes of Language Impairment in a Case of Partial Deletion of NRXN1.
- Published in:
- Molecular Syndromology, 2022, v. 13, n. 6, p. 496, doi. 10.1159/000524710
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- Publication type:
- Article
Language Impairment with a Partial Duplication of DOCK8.
- Published in:
- Molecular Syndromology, 2020, v. 11, n. 5/6, p. 243, doi. 10.1159/000511972
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- Publication type:
- Article
VALORACIÓN DE LA PROGRESIÓN TEMÁTICA EN LA CONVERSACIÓN ESPONTÁNEA DE HABLANTES LESIONADOS DE HEMISFERIO DERECHO.
- Published in:
- Revista de Investigación Lingüística, 2013, v. 16, p. 209
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- Publication type:
- Article
Explicit Oral Narrative Intervention for Students with Williams Syndrome.
- Published in:
- Frontiers in Psychology, 2018, p. 1, doi. 10.3389/fpsyg.2017.02337
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- Publication type:
- Article
Pragmatic Profiles of Adults with Fragile X Syndrome and Williams Syndrome.
- Published in:
- Brain Sciences (2076-3425), 2022, v. 12, n. 3, p. 385, doi. 10.3390/brainsci12030385
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- Publication type:
- Article
Language and Communication Deficits in Chromosome 16p11.2 Deletion Syndrome.
- Published in:
- Journal of Speech, Language & Hearing Research, 2022, v. 65, n. 12, p. 4724, doi. 10.1044/2022_JSLHR-22-00160
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- Publication type:
- Article
Lingüística y déficit comunicativos. ¿Cómo abordar las disfunciones verbales?
- Published in:
- 2017
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- Publication type:
- Book Review