about
Recent advances in the pathogenesis of syndromic autismsDetailed analysis of 22q11.2 with a high density MLPA probe setCharacterizing autism spectrum disorders by key biochemical pathways.Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in miceSept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in miceEvidence for involvement of GNB1L in autism.Acamprosate in a mouse model of fragile X syndrome: modulation of spontaneous cortical activity, ERK1/2 activation, locomotor behavior, and anxietyMolecular mechanisms and diagnosis of chromosome 22q11.2 rearrangementsMouse Models of 22q11.2-Associated Autism Spectrum DisorderGenomic sister-disorders of neurodevelopment: an evolutionary approachEvaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathwaysAssociation testing of copy number variants in schizophrenia and autism spectrum disorders.The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum DisorderNovel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.Age-related gene expression in Tourette syndrome.Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder.Could autism with mental retardation result from digenism and frequent de novo mutations?Autism spectrum disorder in the genetics clinic: a review.Autism spectrum disorders: the quest for genetic syndromes.Medical conditions in autism spectrum disorders22q11.2 microduplication syndrome with associated esophageal atresia/tracheo-esophageal fistula and vascular ringComplex autism spectrum disorder in a patient with a 17q12 microduplicationEpisodic Behavioural Regression in an 8-Year-Old Female: Sequelae of 22q11.2 Duplication SyndromeThe first case of myoclonic epilepsy in a child with a de novo 22q11.2 microduplication
P2860
Q21342782-B2C2AEA2-D851-48CD-89EA-A4AE8A948BFDQ24648626-D1331AF6-250D-4A97-912A-B647C2E54D47Q26781645-DD49B2B5-16B5-4C20-9636-76369A885216Q30439224-E2FBB561-92F2-4CF5-B402-679BBA5EDC16Q30479118-F44D9C55-9A26-47A1-A3CA-2B09689ED545Q30481665-238A0529-8062-4AF8-9516-07A4180B3AD9Q30504581-29101625-3CA7-4B7F-A593-DD7327DAB676Q30855390-3538A239-F0D3-40A3-875C-D957B9B45E04Q33608641-44392CED-F265-4159-A6A4-8A284988567BQ33988040-CBD7D774-12D5-4116-B768-52C4D4ED6EB1Q35960747-D16C1B0B-A6B7-4275-BCFE-AAD8FBC7704BQ36083120-304A28A5-2AE3-4CE5-9F73-906E2C5FA54BQ36217805-964BE64B-9934-4FAC-8AE0-179D2A848C7CQ36499988-D0CE568F-3E38-4D90-9977-07B822C690CFQ36736904-7D86EF0A-B670-46E7-BADB-7F08611A0A39Q37142893-3B7602A2-ABA4-41CE-8B2B-13F80073813AQ37166261-3A90572A-038E-49E1-9B16-0B56908D714AQ37374569-14C191C5-5C71-4C53-8C55-A3B113B0F92AQ38083092-12D84C61-8B86-45AE-B293-22BFC5479294Q38104700-1431F3F4-FF3A-4D0A-BB6C-E3DDE35EE3B8Q38272133-E9D790E4-7266-489A-9181-13559DA0C102Q41785812-CB9CDEED-2582-4D26-A9C0-825D696D157AQ57279132-F9073ECF-4DE3-493D-B5DD-F98E18CCE4EDQ58792881-66284E06-CB00-4240-8C4E-0D322D37252CQ58833704-9FE11262-3F8D-43A3-B081-3764A4CDD5C0
P2860
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
2007年學術文章
@zh-hant
name
Autistic disorder and 22q11.2 duplication.
@en
Autistic disorder and 22q11.2 duplication.
@nl
type
label
Autistic disorder and 22q11.2 duplication.
@en
Autistic disorder and 22q11.2 duplication.
@nl
prefLabel
Autistic disorder and 22q11.2 duplication.
@en
Autistic disorder and 22q11.2 duplication.
@nl
P2860
P1476
Autistic disorder and 22q11.2 duplication.
@en
P2093
Nahit Motavalli Mukaddes
Sabri Herguner
P2860
P304
P356
10.1080/15622970601026701
P577
2007-01-01T00:00:00Z