Found: 8
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Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 4, p. 455, doi. 10.1038/ejhg.2012.165
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- Article
A Diagnostic Marker to Discriminate Childhood Apraxia of Speech From Speech Delay: IV. The Pause Marker Index.
- Published in:
- Journal of Speech, Language & Hearing Research, 2017, v. 60, n. 4, p. S1153, doi. 10.1044/2016_JSLHR-S-16-0149
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- Article
A Diagnostic Marker to Discriminate Childhood Apraxia of Speech From Speech Delay: III. Theoretical Coherence of the Pause Marker with Speech Processing Deficits in Childhood Apraxia of Speech.
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- Journal of Speech, Language & Hearing Research, 2017, v. 60, n. 4, p. S1135, doi. 10.1044/2016_JSLHR-S-15-0298
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- Article
A Diagnostic Marker to Discriminate Childhood Apraxia of Speech From Speech Delay: II. Validity Studies of the Pause Marker.
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- Journal of Speech, Language & Hearing Research, 2017, v. 60, n. 4, p. S1118, doi. 10.1044/2016_JSLHR-S-15-0297
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- Article
A Diagnostic Marker to Discriminate Childhood Apraxia of Speech From Speech Delay: I. Development and Description of the Pause Marker.
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- Journal of Speech, Language & Hearing Research, 2017, v. 60, n. 4, p. S1096, doi. 10.1044/2016_JSLHR-S-15-0296
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- Article
A Diagnostic Marker to Discriminate Childhood Apraxia of Speech From Speech Delay: Introduction.
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- Journal of Speech, Language & Hearing Research, 2017, v. 60, n. 4, p. S1094, doi. 10.1044/2016_JSLHR-S-16-0148
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- Article
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.
- Published in:
- Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-29
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- Article
Phenotype of FOXP2 haploinsufficiency in a mother and son.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 1, p. 174, doi. 10.1002/ajmg.a.34354
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- Article