Contact and support
Need help, have a question, or want to contact the ResearchHub team?
© 2026 ResearchHub. Built for responsible scholarly connection.
Privacy-aware community infrastructureResearch graph
References from Un cas de trouble envahissant du développement avec translocation chromosomique (X ; 4) (p11 ; q13). Local targets link to admitted publications; unresolved targets remain external evidence.
Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q 19q and 22q in Finnish multiplex families
10.1038/sj.mp.4000708 · 2000 · External reference
Association of a balanced chromosomal translocation (4; 12) (q21.3; q15), affective disorder and autism
10.1046/j.1365-2788.2000.00239.x · 2000 · External reference
Asperger's disorder in the emergency psychiatric setting
10.1016/s0163-8343(01)00155-4 · 2001 · External reference
A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2 GLRA3, GLRB) and neuropeptide receptors NPY1R NPY5R
10.1186/1471-2350-5-10 · 2004 · External reference
Case report: autistic disorder and chromosomal abnormality 46 XX duplication (4) p12-p13
10.1007/s007870070035 · 2000 · External reference
