Výsledky vyhledávání - "J A S, Vorstman"

The role of COMT and plasma proline in the variable penetrance of autistic spectrum symptoms in 22q11.2 deletion syndrome

Autor: E, Hidding, H, Swaab, L M J, de Sonneville, H, van Engeland, J A S, Vorstman

Publikováno v: Clinical genetics. 90(5)

This paper examines how COMT

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::453e277a5b1ac43476915546a8d42f3f
https://pubmed.ncbi.nlm.nih.gov/26919535

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Intellectual functioning in relation to autism and ADHD symptomatology in children and adolescents with 22q11.2 deletion syndrome

Autor: E, Hidding, H, Swaab, L M J, de Sonneville, H, van Engeland, M E J, Sijmens-Morcus, P W J, Klaassen, S N, Duijff, J A S, Vorstman

Publikováno v: Journal of intellectual disability research : JIDR. 59(9)

The 22q11.2 deletion syndrome (22q11DS; velo-cardio-facial syndrome) is associated with an increased risk of various disorders, including autism spectrum disorder (ASD) and attention deficit hyperactivity disorder (ADHD). With this study, we aimed to

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1d579a528fa26dd5c079d8921785d23d
https://pubmed.ncbi.nlm.nih.gov/25683771

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Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

Autor: J A S, Vorstman, W G, Staal, E, van Daalen, H, van Engeland, P F R, Hochstenbach, L, Franke

Publikováno v: Molecular psychiatry. 11(1)

The identification of the candidate genes for autism through linkage and association studies has proven to be a difficult enterprise. An alternative approach is the analysis of cytogenetic abnormalities associated with autism. We present a review of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ba3e943fbe00fa13c47091358bfadb20
https://pubmed.ncbi.nlm.nih.gov/16205736

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