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Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNV.
Am J Hum Genet. 2016 Jan 7;98(1):45-57. doi: 10.1016/j.ajhg.2015.11.017. Epub 2015 Dec 31.
Am J Hum Genet. 2016.
PMID: 26749307
Free PMC article.
Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility.
Nuttle X, Giannuzzi G, Duyzend MH, Schraiber JG, Narvaiza I, Sudmant PH, Penn O, Chiatante G, Malig M, Huddleston J, Benner C, Camponeschi F, Ciofi-Baffoni S, Stessman HA, Marchetto MC, Denman L, Harshman L, Baker C, Raja A, Penewit K, Janke N, Tang WJ, Ventura M, Banci L, Antonacci F, Akey JM, Amemiya CT, Gage FH, Reymond A, Eichler EE.
Nuttle X, et al.
Nature. 2016 Aug 11;536(7615):205-9. doi: 10.1038/nature19075. Epub 2016 Aug 3.
Nature. 2016.
PMID: 27487209
Free PMC article.
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Genotype-first analysis of the 16p11.2 deletion defines a new type of "autism".
Duyzend MH, Eichler EE.
Duyzend MH, et al.
Biol Psychiatry. 2015 May 1;77(9):769-71. doi: 10.1016/j.biopsych.2015.02.032. Epub 2015 Mar 2.
Biol Psychiatry. 2015.
PMID: 25843334
Free PMC article.
No abstract available.
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