Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'
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| Veröffentlicht in: | European journal of human genetics : EJHG 2015-09, Vol.23 (9), p.1113-1115 |
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| container_title | European journal of human genetics : EJHG |
| container_volume | 23 |
| creator | 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 |
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| doi_str_mv | 10.1038/ejhg.2014.275 |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 1018-4813 |
| ispartof | European journal of human genetics : EJHG, 2015-09, Vol.23 (9), p.1113-1115 |
| issn | 1018-4813 1476-5438 1476-5438 |
| language | eng |
| recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4538219 |
| source | MEDLINE; EZB-FREE-00999 freely available EZB journals; PubMed Central; SpringerLink Journals - AutoHoldings |
| subjects | 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 |
| title | Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis' |
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