Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'

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Bibliographische Detailangaben
Veröffentlicht in:	European journal of human genetics : EJHG 2015-09, Vol.23 (9), p.1113-1115
Hauptverfasser:	Ceroni, Fabiola, Simpson, Nuala H, Francks, Clyde, Baird, Gillian, Conti-Ramsden, Gina, Clark, Ann, Bolton, Patrick F, Hennessy, Elizabeth R, Donnelly, Peter, Bentley, David R, Martin, Hilary, Parr, Jeremy, Pagnamenta, Alistair T, Maestrini, Elena, Bacchelli, Elena, Fisher, Simon E, Newbury, Dianne F
Format:	Artikel
Sprache:	eng
Schlagworte:	Autism Chromosomes DNA methylation DNA-Binding Proteins - genetics Epigenetics Exons Families & family life Female Hormones Humans Hypotheses Language Development Disorders - genetics Language disorders Letter Male Sequence Deletion Siblings
Online-Zugang:	Volltext
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