Works matching DE "LEARNING disability genetics"
Results: 28
A study of developmental speech and language disorders in twins.
- Published in:
- Journal of Speech & Hearing Research, 1992, v. 35, n. 5, p. 1086, doi. 10.1044/jshr.3505.1086
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- Publication type:
- Article
Gestational age and learning disabilities.
- Published in:
- Developmental Medicine & Child Neurology, 2015, v. 57, n. 5, p. 401, doi. 10.1111/dmcn.12681
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- Publication type:
- Article
Genetic Influences on Learning Disabilities and Speech and Language Disorders.
- Published in:
- Child Development, 1983, v. 54, n. 2, p. 369, doi. 10.2307/1129698
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- Publication type:
- Article
Specific learning disability.
- Published in:
- 2018
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- Publication type:
- journal article
Examining MTSS Implementation Across Systems for SLD Identification: A Case Study.
- Published in:
- 2018
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- Publication type:
- Case Study
Cognitive impairment in preschool children with epilepsy.
- Published in:
- Epilepsia (Series 4), 2011, v. 52, n. 8, p. 1499, doi. 10.1111/j.1528-1167.2011.03092.x
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- Publication type:
- Article
Should We Undertake Genetic Research on Intelligence?
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- Bioethics, 1999, v. 13, n. 3/4, doi. 10.1111/1467-8519.00161
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- Publication type:
- Article
Characterizing the ADHD phenotype for genetic studies.
- Published in:
- Developmental Science, 2005, v. 8, n. 2, p. 115, doi. 10.1111/j.1467-7687.2005.00398.x
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- Publication type:
- Article
Genetics of developmental dyslexia.
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- European Child & Adolescent Psychiatry, 2010, v. 19, n. 3, p. 179, doi. 10.1007/s00787-009-0081-0
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- Publication type:
- Article
Deletion in Xp22.11: PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism.
- Published in:
- Clinical Genetics, 2011, v. 79, n. 1, p. 79, doi. 10.1111/j.1399-0004.2010.01590.x
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- Publication type:
- Article
Reading and Writing Skills in Children With Specific Learning Disabilities With and Without Developmental Coordination Disorder.
- Published in:
- 2018
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- Publication type:
- journal article
Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects.
- Published in:
- Behavior Genetics, 2011, v. 41, n. 1, p. 90, doi. 10.1007/s10519-010-9424-3
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- Publication type:
- Article
An Examination of Candidate Gene SNPs for Dyslexia in an Indian Sample.
- Published in:
- Behavior Genetics, 2011, v. 41, n. 1, p. 105, doi. 10.1007/s10519-010-9441-2
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- Publication type:
- Article
SNP Variations in the 7q33 Region Containing DGKI are Associated with Dyslexia in the Finnish and German Populations.
- Published in:
- Behavior Genetics, 2011, v. 41, n. 1, p. 134, doi. 10.1007/s10519-010-9431-4
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- Publication type:
- Article
Moving Closer to a Public Health Model of Language and Learning Disabilities: The Role of Genetics and the Search for Etiologies.
- Published in:
- Behavior Genetics, 2011, v. 41, n. 1, p. 1, doi. 10.1007/s10519-010-9439-9
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- Publication type:
- Article
An Application of the Elastic Net for an Endophenotype Analysis.
- Published in:
- Behavior Genetics, 2011, v. 41, n. 1, p. 120, doi. 10.1007/s10519-011-9443-8
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- Publication type:
- Article
In Search of the Perfect Phenotype: An Analysis of Linkage and Association Studies of Reading and Reading-Related Processes.
- Published in:
- Behavior Genetics, 2011, v. 41, n. 1, p. 6, doi. 10.1007/s10519-011-9444-7
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- Publication type:
- Article
Genome Scan for Spelling Deficits: Effects of Verbal IQ on Models of Transmission and Trait Gene Localization.
- Published in:
- Behavior Genetics, 2011, v. 41, n. 1, p. 31, doi. 10.1007/s10519-010-9390-9
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- Publication type:
- Article
Strain Differences in Rewarded Discrimination Learning Using the Olfactory Tubing Maze.
- Published in:
- Behavior Genetics, 2006, v. 36, n. 6, p. 923, doi. 10.1007/s10519-006-9088-1
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- Publication type:
- Article
Using Discrete Trial Training to Identify Specific Learning Impairments in Boys with Fragile X Syndrome.
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- Journal of Autism & Developmental Disorders, 2014, v. 44, n. 7, p. 1659, doi. 10.1007/s10803-014-2037-6
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- Publication type:
- Article
Validation of a Screening Tool for Learning Disorder in Children.
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- Indian Journal of Psychological Medicine, 2017, v. 39, n. 6, p. 737, doi. 10.4103/IJPSYM.IJPSYM_29_17
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- Publication type:
- Article
Complex Rearrangement Involving Three Chromosomes, Four Breakpoints and a 2.7-Mb Deletion in the 18q Segment Observed in a Girl with Mild Learning Difficulties.
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- Cytogenetic & Genome Research, 2016, v. 147, n. 2/3, p. 118, doi. 10.1159/000442583
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- Publication type:
- Article
Mechanism for the learning deficits in a mouse model of neurofibromatosis type 1.
- Published in:
- Nature, 2002, v. 415, n. 6871, p. 526, doi. 10.1038/nature711
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- Publication type:
- Article
Difference and choice: exploring prenatal testing and the use of genetic information with people with learning difficulties.
- Published in:
- British Journal of Learning Disabilities, 2002, v. 30, n. 2, p. 50, doi. 10.1046/j.1468-3156.2002.00164.x
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- Publication type:
- Article
The cognitive profiles of Jordanian students at risk for math disability.
- Published in:
- International Journal of Inclusive Education, 2018, v. 22, n. 10, p. 1093, doi. 10.1080/13603116.2017.1415382
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- Publication type:
- Article
Attention-deficit/hyperactivity disorder associated with KChIP1 rs1541665 in Kv channels accessory proteins.
- Published in:
- PLoS ONE, 2017, v. 12, n. 11, p. 1, doi. 10.1371/journal.pone.0188678
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- Publication type:
- Article
A Parent's Experience of Schooling for a Child with Prader-Willi Syndrome.
- Published in:
- Reach, 2009, v. 23, n. 1, p. 24
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- Publication type:
- Article
Characterization of two familial cases presenting with a syndromic specific learning disorder and carrying (17q;21q) unbalanced translocations.
- Published in:
- Clinical Case Reports, 2018, v. 6, n. 5, p. 827, doi. 10.1002/ccr3.1450
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- Publication type:
- Article