Pages that link to "Q51925060"

The following pages link to Further evidence of pleiotropy influencing speech and language: analysis of the DYX8 region. (Q51925060):

Displaying 19 items.

• Genetic Advances in the Study of Speech and Language Disorders (Q24609855) (← links)
• The genetics of reading disabilities: from phenotypes to candidate genes (Q30459192) (← links)
• A multigenerational family study of oral and hand motor sequencing ability provides evidence for a familial speech sound disorder subtype (Q30469175) (← links)
• The complex of TFII-I, PARP1, and SFPQ proteins regulates the DYX1C1 gene implicated in neuronal migration and dyslexia (Q30482949) (← links)
• Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment (Q30492191) (← links)
• Literacy outcomes of children with early childhood speech sound disorders: impact of endophenotypes (Q30522146) (← links)
• Speaking genes or genes for speaking? Deciphering the genetics of speech and language (Q33939634) (← links)
• A common haplotype of KIAA0319 contributes to the phonological awareness skill in Chinese children (Q33965244) (← links)
• Association between AVPR1A, DRD2, and ASPM and endophenotypes of communication disorders (Q34078987) (← links)
• Etiologies and Molecular Mechanisms of Communication Disorders (Q34146699) (← links)
• Motor sequencing deficit as an endophenotype of speech sound disorder: a genome-wide linkage analysis in a multigenerational family (Q36125741) (← links)
• Pleiotropic effects of DCDC2 and DYX1C1 genes on language and mathematics traits in nuclear families of developmental dyslexia. (Q37612214) (← links)
• Speech-language pathology insights into genetics and neuroscience: beyond surface behaviour (Q38099014) (← links)
• Children with comorbid speech sound disorder and specific language impairment are at increased risk for attention-deficit/hyperactivity disorder. (Q38394969) (← links)
• An Analytic Solution to the Computation of Power and Sample Size for Genetic Association Studies under a Pleiotropic Mode of Inheritance (Q38896201) (← links)
• Non-nuclear Pool of Splicing Factor SFPQ Regulates Axonal Transcripts Required for Normal Motor Development (Q41985778) (← links)
• A Cohort of Balanced Reciprocal Translocations Associated with Dyslexia: Identification of Two Putative Candidate Genes at DYX1 (Q58612547) (← links)
• A frequent acoustic sign of speech motor delay (SMD) (Q92840127) (← links)
• Initial studies of the phenotype and persistence of speech motor delay (SMD) (Q92910512) (← links)