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Female with autistic disorder and monosomy X (Turner syndrome): Parent-of-origin effect of the X chromosome
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“with an increased rate of ASD diagnosis in Turner syndrome (TS, XO, ~3% ASD) [52,53,54], Klinefelter syndrome (KS, XXY, ~10% ASD) [55,56*], and 47,XYY syndrome (~20% ASD), but no increased rate in X chromosome trisomy [57,58**].”
From Sex differences in autism spectrum disorders (2013) · cites this paper as [52]
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“in patients with MDD, there appears to be no general association between the disease and this SNP (Desan et al., 2000).”
From Circadian genes, rhythms and the biology of mood disorders (2007) · cites this paper as Desan et al., 2000
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Genetic Overlap Between Measures of Hyperactivity/Inattention and Mood in Children and Adolescents
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The Molecular Neurobiology of Twelve Steps Program & Fellowship: Connecting the Dots for Recovery
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Metadata
- Authors
- Donnelly, S. L., Wolpert, C. M., Menold, M. M., Bass, M. P., Gilbert, J. R., Cuccaro, M. L., Delong, G. R., & Pericak-Vance, M. A.
- Venue
- American Journal of Medical Genetics
- Published
- 2000
- References
- 49
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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