Found: 8
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Association between autism and variants in the wingless-type MMTV integration site family member 2 (WNT2) gene.
- Published in:
- International Journal of Neuropsychopharmacology, 2010, v. 13, n. 4, p. 443, doi. 10.1017/S1461145709990903
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- Article
Association of the oxytocin receptor (OXTR) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population.
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- Journal of Human Genetics, 2010, v. 55, n. 3, p. 137, doi. 10.1038/jhg.2009.140
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- Article
No evidence for significant association between GABA receptor genes in chromosome 15q11–q13 and autism in a Japanese population.
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- Journal of Human Genetics, 2007, v. 52, n. 12, p. 985, doi. 10.1007/s10038-007-0207-5
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- Article
No association between the ryanodine receptor 3 gene and autism in a Japanese population.
- Published in:
- Psychiatry & Clinical Neurosciences, 2008, v. 62, n. 3, p. 341, doi. 10.1111/j.1440-1819.2008.01802.x
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- Article
Linkage Analysis between Familial Myoclonus Epilepsy and Short Arm of Chromosome 6 Using HLA Phenotype as Genetic Marker.
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- Psychiatry & Clinical Neurosciences, 1993, v. 47, n. 2, p. 275, doi. 10.1111/j.1440-1819.1993.tb02071.x
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- Article
A Case of Non-24-Hour Sleep-Wake Syndrome Preceded by Depressive State.
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- Psychiatry & Clinical Neurosciences, 1990, v. 44, n. 1, p. 191, doi. 10.1111/j.1440-1819.1990.tb00484.x
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- Article
Identification of Four Novel Synonymous Substitutions in the X-Linked Genes Neuroligin 3 and Neuroligin 4X in Japanese Patients with Autistic Spectrum Disorder.
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- Autism Research & Treatment, 2012, p. 1, doi. 10.1155/2012/724072
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- Article
A Family with an atonic variant of paroxysmal kinesigenic choreoathetosis and hypercalcitoninemia.
- Published in:
- Movement Disorders, 1999, v. 14, n. 2, p. 342, doi. 10.1002/1531-8257(199903)14:2<342::AID-MDS1022>3.0.CO;2-7
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- Article