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British Journal of Psychiatry, ISSN 0007-1250, 01/2012, Volume 200, Issue 1, pp. 14 - 14
Journal Article
The British journal of psychiatry : the journal of mental science, ISSN 0007-1250, 01/2012, Volume 200, Issue 1, pp. 14 - 14
Journal Article
PLOS Genetics, ISSN 1553-7390, 2013, Volume 9, Issue 9, p. e1003751
Humans display structural and functional asymmetries in brain organization, strikingly with respect to language and handedness. The molecular basis of these... 
SITUS-INVERSUS | LATERALITY | DYSLEXIA | CORPUS-CALLOSUM | RIGHT-HANDEDNESS | MOUSE | GENETICS & HEREDITY | SCHIZOPHRENIA | MOTOR COORDINATION | GENOME-WIDE ASSOCIATION | CURRENT ISSUES | Human mechanics | Genetic aspects | Research | Gene expression | Symmetry (Biology) | Genetic variation | Confidence intervals | Handedness | Brain research | Language | Asymmetry | Councils | Genes | Bias | Population | Dyslexia | Genomes
Journal Article
Nature Genetics, ISSN 1061-4036, 03/2017, Volume 49, Issue 4, pp. 559 - 567
Journal Article
Journal Article
Journal Article
Translational Psychiatry, ISSN 2158-3188, 12/2019, Volume 9, Issue 1, pp. 77 - 15
Journal Article
Human molecular genetics, 08/2018, Volume 27, Issue 16, p. 2775
Winchester syndrome (WS, MIM #277950) is an extremely rare autosomal recessive skeletal dysplasia characterized by progressive joint destruction and... 
Journal Article
PLoS ONE, ISSN 1932-6203, 11/2012, Volume 7, Issue 11, p. e50321
Independent studies have shown that candidate genes for dyslexia and specific language impairment (SLI) impact upon reading/language-specific traits in the... 
LANGUAGE | POPULATION | HUMAN INTELLIGENCE | GENETICS | MULTIDISCIPLINARY SCIENCES | ARCHITECTURE | SPEECH | MICROSTRUCTURE | GENOME-WIDE ASSOCIATION | WORKING-MEMORY | CHILDREN | Chromosomes, Human, Pair 2 - ultrastructure | Haplotypes | Humans | Middle Aged | Open Reading Frames | Child, Preschool | Male | Brain - physiology | Diagnostic Imaging - methods | Dyslexia - physiopathology | Language | Cognition - physiology | Adult | Female | Neurons - metabolism | Child | Risk Factors | Genotype | Brain Mapping - methods | Models, Statistical | Dyslexia - genetics | Intelligence Tests | Phenotype | Adolescent | Models, Genetic | Polymorphism, Single Nucleotide | Cohort Studies | Medicine, Experimental | Medical research | Dyslexia | Research | Genes | Risk factors | Neurosciences | Memory | Cognitive ability | Childrens health | Parents | Families & family life | Genomes | Literacy | Cortex (parietal) | Genetics | Cingulum | Children | Chromosomes | Cortex (temporal) | Language disorders | Statistical analysis | Nutrition | Cortex (occipital) | Risk analysis | Substantia alba | Chromosome 2 | Loci | Corpus callosum | Children & youth | Lobes | Studies | Genetic variance | Reading | Brain research | Correlation analysis | Basic Medicine | Medical Genetics | Medicinsk genetik | Molecular Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Molekylär genetik
Journal Article