Výsledky vyhľadávania - "Dyslexia diagnostic imaging"

Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family

Autori: Clyde Francks Barbara Franke Ben Maassen a ďalší

Zdroj: Hum Genet
Addi. Archivo Digital para la Docencia y la Investigación
Universidad del País Vasco
instname
Human Genetics, 140, 8, pp. 1183-1200
Human Genetics

Predmety: Neuroinformatics, Male, 0301 basic medicine, Genetic Linkage, Neurons/metabolism, Inheritance Patterns, Gene Expression, Neuroimaging, Chromosomes, Dyslexia, 03 medical and health sciences, Cell Movement, Humans, Dominant, Family, Genetic Predisposition to Disease, Polymorphism, Original Investigation, Genes, Dominant, Neurons, 0303 health sciences, Semaphorins/deficiency, Radboudumc 7: Neurodevelopmental disorders DCMN: Donders Center for Medical Neuroscience, Whole Genome Sequencing, Base Sequence, Dyslexia/diagnostic imaging, Polymorphism, Single Nucleotide [MeSH], Cell Movement [MeSH], Molecular Medicine, Gene Expression [MeSH], Male [MeSH], Semaphorins/deficiency [MeSH], Neuroimaging [MeSH], Phenotype [MeSH], Base Sequence [MeSH], Lod Score [MeSH], Introns [MeSH], Human Genetics, Genetic Predisposition to Disease [MeSH], Chromosomes, Human, Pair 7 [MeSH], Female [MeSH], Whole Genome Sequencing [MeSH], Dyslexia/genetics [MeSH], Humans [MeSH], Inheritance Patterns [MeSH], Neurons/metabolism [MeSH], Genes, Dominant [MeSH], Family [MeSH], Genetic Linkage [MeSH], Dyslexia/metabolism [MeSH], Genome-Wide Association Study [MeSH], Genetic Loci [MeSH], Dyslexia/diagnostic imaging [MeSH], Pedigree [MeSH], Metabolic Diseases, Semaphorins/genetics [MeSH], Gene Function, Neurons/pathology [MeSH], Dyslexia/physiopathology [MeSH], Haplotypes [MeSH], Single Nucleotide, Introns, Pedigree, Phenotype, Genes, Haplotypes, Genetic Loci, Pair 7, Female, Lod Score, Chromosomes, Human, Pair 7, Human, Genome-Wide Association Study

Popis súboru: application/pdf; application/vnd.openxmlformats-officedocument.spreadsheetml.sheet

Prístupová URL adresa: https://link.springer.com/content/pdf/10.1007/s00439-021-02289-w.pdf
https://pubmed.ncbi.nlm.nih.gov/34076780
http://hdl.handle.net/10810/53361
https://pure.mpg.de/pubman/item/item_3316961_3/component/file_3329901/Carrion-Castillo_etal_2021_Whole-genome%20sequencing%20identifies%20functional....pdf
https://addi.ehu.es/handle/10810/53361
https://europepmc.org/article/MED/34076780
https://pubmed.ncbi.nlm.nih.gov/34076780/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8263547
https://pure.mpg.de/pubman/faces/ViewItemOverviewPage.jsp?itemId=item_3316961
https://repository.ubn.ru.nl/handle/2066/237920
https://repository.ubn.ru.nl//bitstream/handle/2066/237920/237920.pdf
http://hdl.handle.net/21.11116/0000-0008-A0B4-7
http://hdl.handle.net/21.11116/0000-0008-A0B5-6
http://hdl.handle.net/21.11116/0000-0008-D6D3-8
http://hdl.handle.net/21.11116/0000-0008-A0B1-A
https://repository.publisso.de/resource/frl:6446840

Left and right in the brain - specialization for auditory signals and and linguistic sounds? / Venstre og höyre i hjernen - spesialisering for auditive signaler og språklige lyder?

Autori: Hugdahl, K

Zdroj: AudioNytt. 26(1-2):30

Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family

Autori: Carrion-Castillo, Amaia Estruch, Sara B. Maassen, Ben a ďalší

Zdroj: Carrion-Castillo, A, Estruch, S B, Maassen, B, Franke, B, Francks, C & Fisher, S E 2021, 'Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family', HUMAN GENETICS, vol. 140, no. 8, pp. 1183-1200.

Témy: Base Sequence, Cell Movement, Chromosomes, Human, Pair 7, Dyslexia/diagnostic imaging, Family, Female, Gene Expression, Genes, Dominant, Genetic Linkage, Genetic Loci, Genetic Predisposition to Disease, Genome-Wide Association Study, Haplotypes, Humans, Inheritance Patterns, Introns, Lod Score, Male, Neuroimaging, Neurons/metabolism, Pedigree, Phenotype, Polymorphism, Single Nucleotide, Semaphorins/deficiency, Whole Genome Sequencing, article

URL: https://research.rug.nl/en/publications/18f188fa-d24d-49ea-9771-8c40c02b535f
https://doi.org/10.1007/s00439-021-02289-w
https://hdl.handle.net/11370/18f188fa-d24d-49ea-9771-8c40c02b535f
https://pure.rug.nl/ws/files/176114252/Whole_genome_sequencing_identifies_functional_noncoding_variation_in_SEMA3C_that_cosegregates_with_dyslexia_in_a_multigenerational_family.pdf
https://www.scopus.com/pages/publications/85107147596
info:eu-repo/semantics/altIdentifier/doi/10.1007/s00439-021-02289-w
info:eu-repo/semantics/altIdentifier/pmid/34076780
info:eu-repo/semantics/altIdentifier/wos/000657231700001
info:eu-repo/semantics/altIdentifier/hdl/https://hdl.handle.net/11370/18f188fa-d24d-49ea-9771-8c40c02b535f
info:eu-repo/semantics/altIdentifier/pissn/0340-6717