Epigenotype–genotype–phenotype correlations in <i>SETD1A</i> and <i>SETD2</i> chromatin disorders
- DOI
- 10.1093/hmg/ddad079
- Published
- 2023-05-11
- Container
- Human Molecular Genetics
- Publisher
- Oxford University Press (OUP)
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1093/hmg/ddad079,
title = {Epigenotype–genotype–phenotype correlations in <i>SETD1A</i> and <i>SETD2</i> chromatin disorders},
author = {Sunwoo Lee and Lara Menzies and Eleanor Hay and Eguzkine Ochoa and France Docquier and Fay Rodger and Charu Deshpande and Nicola C Foulds and Sébastien Jacquemont and Khadije Jizi and Henriette Kiep and Alison Kraus and Katharina Löhner and Patrick J Morrison and Bernt Popp and Ruth Richardson and Arie van Haeringen and Ezequiel Martin and Ana Toribio and Fudong Li and Wendy D Jones and Francis H Sansbury and Eamonn R Maher},
year = {2023},
journal = {Human Molecular Genetics},
doi = {10.1093/hmg/ddad079},
url = {https://doi.org/10.1093/hmg/ddad079}
}RIS
TY - JOUR TI - Epigenotype–genotype–phenotype correlations in <i>SETD1A</i> and <i>SETD2</i> chromatin disorders AU - Sunwoo Lee AU - Lara Menzies AU - Eleanor Hay AU - Eguzkine Ochoa AU - France Docquier AU - Fay Rodger AU - Charu Deshpande AU - Nicola C Foulds AU - Sébastien Jacquemont AU - Khadije Jizi AU - Henriette Kiep AU - Alison Kraus AU - Katharina Löhner AU - Patrick J Morrison AU - Bernt Popp AU - Ruth Richardson AU - Arie van Haeringen AU - Ezequiel Martin AU - Ana Toribio AU - Fudong Li AU - Wendy D Jones AU - Francis H Sansbury AU - Eamonn R Maher PY - 2023 JO - Human Molecular Genetics DO - 10.1093/hmg/ddad079 UR - https://doi.org/10.1093/hmg/ddad079 ER -
APA
Lee, S., Menzies, L., Hay, E., Ochoa, E., Docquier, F., Rodger, F., Deshpande, C., Foulds, N. C., Jacquemont, S., Jizi, K., Kiep, H., Kraus, A., Löhner, K., Morrison, P. J., Popp, B., Richardson, R., Haeringen, A. V., Martin, E., Toribio, A., Li, F., Jones, W. D., Sansbury, F. H., & Maher, E. R. (2023). Epigenotype–genotype–phenotype correlations in <i>SETD1A</i> and <i>SETD2</i> chromatin disorders. Human Molecular Genetics. https://doi.org/10.1093/hmg/ddad079
Source records
- crossref · retrieved 2026-09-27T16:27:52.095Z