Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
https://www.nature.com/articles/s41431-021-01018-1.pdf
Reference34 articles.
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2. May M, Colleaux L, Murgia A, Aylsworth A, Nussbaum R, Fontes M, et al. Molecular analysis of four males with mental retardation and deletions of Xq21 places the putative MR region in Xq21.1 between DXS233 and CHM. Hum Mol Genet. 1995;4:1465–6.
3. Tarpey PS, Smith R, Pleasance E, Whibley A, Edkins S, Hardy C, et al. A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. Nat Genet. 2009;41:535–43.
4. van der Werf IM, Dijck AV, Reyniers E, Helsmoortel C, Kumar AA, Kalscheuer VM, et al. Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability. Gene. 2017;605:92–8.
5. Delphin N, Hanein S, Taie LF, Zanlonghi X, Bonneau D, Moisan JP, et al. Intellectual disability associated with retinal dystrophy in the Xp11.3 deletion syndrome: ZNF674 on trial. Guilty or innocent? Eur J Hum Genet. 2012;20:352–6.
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1. Correction: Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711;European Journal of Human Genetics;2023-12-01
2. Clinical findings in individuals with duplication of genes associated with X‐linked intellectual disability;Clinical Genetics;2023-10-29
3. Genome-wide CNV analysis uncovers novel pathogenic regions in cohort of five multiplex families with neurodevelopmental disorders;Heliyon;2023-09
4. Regulatory Start-Stop Elements in 5’ Untranslated Regions Pervasively Modulate Translation;2023
5. Identification of DCAF1 by Clinical Exome Sequencing and Methylation Analysis as a Candidate Gene for Autism and Intellectual Disability: A Case Report;Journal of Personalized Medicine;2022-05-27
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