A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency.
about
Genetics of dyslexia: the evolving landscapeDifferential Diagnosis of Dysgraphia, Dyslexia, and OWL LD: Behavioral and Neuroimaging Evidence.Association of short-term memory with a variant within DYX1C1 in developmental dyslexiaGlobal processing speed in children with low reading ability and in children and adults with typical reading ability: exploratory factor analytic models.The genetics of reading disabilities: from phenotypes to candidate genesGenome scan for cognitive trait loci of dyslexia: Rapid naming and rapid switching of letters, numbers, and colorsConverging evidence for triple word form theory in children with dyslexia.Tract-based spatial statistics of diffusion tensor imaging in adults with dyslexiaBrain classification reveals the right cerebellum as the best biomarker of dyslexia.Identification of candidate genes for dyslexia susceptibility on chromosome 18.Predicting Levels of Reading and Writing Achievement in Typically Developing, English-Speaking 2(nd) and 5(th) Graders.Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci.A genomewide scan for intelligence identifies quantitative trait loci on 2q and 6p.Evidence-based diagnosis and treatment for specific learning disabilities involving impairments in written and/or oral language.Comorbidity of ADHD and dyslexia.A theoretical molecular network for dyslexia: integrating available genetic findings.Inter-relationships among behavioral markers, genes, brain and treatment in dyslexia and dysgraphiaGenome scan for spelling deficits: effects of verbal IQ on models of transmission and trait gene localization.Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17.In search of the perfect phenotype: an analysis of linkage and association studies of reading and reading-related processes.A multidisciplinary approach to understanding developmental dyslexia within working-memory architecture: genotypes, phenotypes, brain, and instruction.Evidence-Based Reading and Writing Assessment for Dyslexia in Adolescents and Young Adults.Writing problems in developmental dyslexia: under-recognized and under-treatedGenomewide scan for real-word reading subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity.Molecular genetics of dyslexia: an overview.Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample.Do Dyslexics Misread a ROWS for a ROSE?Familial dyskinesia and facial myokymia (FDFM): Follow-up of a large family and linkage to chromosome 3p21-3q21.Teaching children with dyslexia to spell in a reading-writers' workshop.Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36.Genetic risk variants for dyslexia on chromosome 18 in a German cohort.SNP sets and reading ability: testing confirmation of a 10-SNP set in a population sample.Interrelationship and familiality of dyslexia related quantitative measures.
P2860
Q22306529-E556CE8F-54A8-4130-881D-0D27D3C0313CQ27314525-CE68ED3E-B6CD-44EE-A1CD-B48D8312255FQ28288962-0863AD5F-13DB-4601-AA0F-DC82BF81A713Q30445351-BBAE1397-11D6-4672-8CE0-C3C72DE6010EQ30459192-2797D20D-9B4B-4A9F-BB34-EABB3B3D4E44Q30580481-53C18E40-3733-4F2C-8163-A9CF5EEC0A4CQ31056187-0D05989F-5AA7-4949-8A0D-DB0F64861356Q31155021-BBA0B01C-50E9-42FB-85E0-88F116F6ED7BQ33474551-66FA0854-E4C9-4A49-9175-5AB5EA97F3F4Q33742226-80007E4E-732E-40DE-9F44-230B7B4B661FQ33758520-507B7FED-431C-44C7-BD0B-84757A4C1ACFQ33785862-BD6EDBAB-D8D3-4E07-8A9C-CD5CC0B7F039Q34015456-67F4B19B-FB12-43AA-A8C1-8ED994B17D7FQ34025987-755DEF58-014A-4B7F-91A1-DED65B53D30CQ34132050-1873078F-2247-4314-9BC4-7A85BC2127B8Q34144455-CA85EA83-4881-48D1-B41E-601B3B3A89FCQ34193229-97A30175-E2FD-4A1A-980E-20CE1AF77C5CQ34538356-81485C2B-149D-4B37-8319-8D8E5ED7B8D3Q34583528-F0C3B93F-310E-4182-A431-EF846EA2DDE9Q34666100-D350FC0A-0554-4EC2-B981-EA7CC03EBA0BQ34879093-D37D7D41-17E6-49E1-BE3F-BF41E4E4D478Q36539865-66F043E0-DB20-4230-AE3C-D53A591B6EE0Q36591862-15A71F2A-2A57-42D2-9ABE-ABD5EEBC2168Q36916885-8D2505DC-A1CE-47AF-8947-534EDA0B2B30Q38153350-F00D2FF2-70AB-4019-BC1B-B37B4ECD4923Q38271952-8DD7EC49-9C7E-4D3F-93BF-16B65AC0A2CFQ38455434-CE4DA842-C380-4316-B96B-D61E3B32205EQ42020018-E1AADF90-79E6-48E1-9448-E3289D4BC0C8Q44684985-E3F329EF-CD92-488B-B1F4-5D3608FC64E4Q48276055-B9845E31-FCE0-4620-8C00-DFCAC692C4FDQ50738677-2DF8F5AC-5E41-4D7D-B5BB-D6378C2CD0A3Q51548524-5018D42E-E94E-4068-A949-BF2C54841035Q51931161-2FF4439F-449E-4769-9CDC-4C470413B0AC
P2860
A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh-hant
name
A genome scan in multigenerati ...... nological decoding efficiency.
@en
A genome scan in multigenerati ...... nological decoding efficiency.
@nl
type
label
A genome scan in multigenerati ...... nological decoding efficiency.
@en
A genome scan in multigenerati ...... nological decoding efficiency.
@nl
prefLabel
A genome scan in multigenerati ...... nological decoding efficiency.
@en
A genome scan in multigenerati ...... nological decoding efficiency.
@nl
P2093
P2860
P356
P1433
P1476
A genome scan in multigenerati ...... nological decoding efficiency.
@en
P2093
Berninger VW
Chapman NH
Matsushita M
Raskind WH
Thomson JB
Wijsman EM
P2860
P2888
P304
P356
10.1038/SJ.MP.4001657
P407
P577
2005-07-01T00:00:00Z