Hits 13.041 – 13.060 of 13.112
13045 |
Identifying Children at Risk for Language Impairment or Dyslexia With Group-Administered Measures.
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13046 |
A longitudinal study on predictors of early calculation development among young children at risk for learning difficulties.
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13047 |
Reconsidering the simple view of reading in an intriguing case of equivalent models: commentary on Tunmer and Chapman (2012).
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13049 |
A balanced t(10;15) translocation in a male patient with developmental language disorder.
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Ercan-Sencicek, A Gulhan (authoraut); Davis Wright, Nicole R (authoraut); Sanders, Stephan J (authoraut); Oakman, Nicole (authoraut); Valdes, Lianna (authoraut); Bakkaloglu, Betul (authoraut); Doyle, Niamh (authoraut); Yrigollen, Carolyn M (authoraut); Morgan, Thomas M (authoraut); Grigorenko, Elena L (authoraut)
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Abstract:
We report the clinical and cytogenetic findings on a male child with developmental language disorder, no physical abnormalities, and a balanced t(10;15)(q24.1;q21.1) translocation. As the child's parents are unavailable for investigations, it is unclear whether the translocation is inherited or de novo. Fluorescence in situ hybridization (FISH) analyses were carried out using specific RP11-BAC clones mapping near 15q21.1 and 10q24.1 to refine the location of the breakpoints. The breakpoint on 15q21.1 interrupts the SEMA6D gene and the breakpoint on 10q24.1 is located between the ENTPD1 and CCNJ genes. The SEMA6D gene was further investigated in samples of individuals with developmental language disorders and controls; this investigation offered further evidence of the involvement of SEMA6D with developmental language disorders. ; DC007665, HD052120, P50 HD052120, P50 HD052120-05, R01 DC007665, R01 DC007665-05 ; This NIH-funded author manuscript originally appeared in PubMed Central at http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3322462.
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Keyword:
Child; Chromosome Breakpoints; Chromosomes; Fluorescence; Genetic; Human; Humans; In Situ Hybridization; Language Development Disorders/genetics; Male; Pair 10; Pair 15; Semaphorins/genetics; Translocation
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URL: http://purl.flvc.org/fsu/fd/FSU_pmch_22266071 http://diginole.lib.fsu.edu/islandora/object/fsu%3A330507/datastream/TN/view/balanced%20t%2810%3B15%29%20translocation%20in%20a%20male%20patient%20with%20developmental%20language%20disorder.jpg https://doi.org/10.1016/j.ejmg.2011.12.005
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13050 |
An evaluation of two emergent literacy screening tools for preschool children.
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13051 |
Identifying preschool children at risk of later reading difficulties: evaluation of two emergent literacy screening tools.
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13052 |
Identifying learning patterns of children at risk for Specific Reading Disability.
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13053 |
Attentional but not pre-attentive neural measures of auditory discrimination are atypical in children with developmental language disorder.
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13054 |
Neural preservation underlies speech improvement from auditory deprivation in young cochlear implant recipients.
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13055 |
Lexical leverage: category knowledge boosts real-time novel word recognition in 2-year-olds.
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13056 |
Maternal Socioeconomic Status Influences the Range of Expectations During Language Comprehension in Adulthood.
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13057 |
Spelling well despite developmental language disorder: what makes it possible?
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13058 |
Lexical processing deficits in children with developmental language disorder: An event-related potentials study.
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13059 |
Predictive validity of the get ready to read! Screener: concurrent and long-term relations with reading-related skills.
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13060 |
Gender and agreement processing in children with developmental language disorder.
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