Syndromic neurodevelopmental disorder associated with de novo variants in <scp> <i>DDX23</i> </scp>

William Burns, Lynne M. Bird, Delphine Heron, Boris Keren, Divya Ramachandra, Isabelle Thiffault, Florencia Del Viso, Shivarajan Amudhavalli, Kendra Engleman, Ilaria Parenti, Frank J. Kaiser, Jolanta Wierzba, Korbinian M. Riedhammer, Susanne Liptay, Neda Zadeh, Joseph Porrmann, Andrea Fischer, Sophie Gößwein, Heather M. McLaughlin, Aida Telegrafi, Katherine G. Langley, Richard Steet, Raymond J. Louie, Michael J. Lyons

Open source

DOI: 10.1002/ajmg.a.62359
Published: 2021-05-29
Container: American Journal of Medical Genetics Part A
Publisher: Wiley
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1002/ajmg.a.62359,
  title = {Syndromic neurodevelopmental disorder associated with de novo variants in
                    <scp>
                      <i>DDX23</i>
                    </scp>},
  author = {William Burns and Lynne M. Bird and Delphine Heron and Boris Keren and Divya Ramachandra and Isabelle Thiffault and Florencia Del Viso and Shivarajan Amudhavalli and Kendra Engleman and Ilaria Parenti and Frank J. Kaiser and Jolanta Wierzba and Korbinian M. Riedhammer and Susanne Liptay and Neda Zadeh and Joseph Porrmann and Andrea Fischer and Sophie Gößwein and Heather M. McLaughlin and Aida Telegrafi and Katherine G. Langley and Richard Steet and Raymond J. Louie and Michael J. Lyons},
  year = {2021},
  journal = {American Journal of Medical Genetics Part A},
  doi = {10.1002/ajmg.a.62359},
  url = {https://doi.org/10.1002/ajmg.a.62359}
}

RIS

TY  - JOUR
TI  - Syndromic neurodevelopmental disorder associated with de novo variants in
                    <scp>
                      <i>DDX23</i>
                    </scp>
AU  - William Burns
AU  - Lynne M. Bird
AU  - Delphine Heron
AU  - Boris Keren
AU  - Divya Ramachandra
AU  - Isabelle Thiffault
AU  - Florencia Del Viso
AU  - Shivarajan Amudhavalli
AU  - Kendra Engleman
AU  - Ilaria Parenti
AU  - Frank J. Kaiser
AU  - Jolanta Wierzba
AU  - Korbinian M. Riedhammer
AU  - Susanne Liptay
AU  - Neda Zadeh
AU  - Joseph Porrmann
AU  - Andrea Fischer
AU  - Sophie Gößwein
AU  - Heather M. McLaughlin
AU  - Aida Telegrafi
AU  - Katherine G. Langley
AU  - Richard Steet
AU  - Raymond J. Louie
AU  - Michael J. Lyons
PY  - 2021
JO  - American Journal of Medical Genetics Part A
DO  - 10.1002/ajmg.a.62359
UR  - https://doi.org/10.1002/ajmg.a.62359
ER  -

APA

Burns, W., Bird, L. M., Heron, D., Keren, B., Ramachandra, D., Thiffault, I., Viso, F. D., Amudhavalli, S., Engleman, K., Parenti, I., Kaiser, F. J., Wierzba, J., Riedhammer, K. M., Liptay, S., Zadeh, N., Porrmann, J., Fischer, A., Gößwein, S., McLaughlin, H. M., Telegrafi, A., Langley, K. G., Steet, R., Louie, R. J., & Lyons, M. J. (2021). Syndromic neurodevelopmental disorder associated with de novo variants in <scp> <i>DDX23</i> </scp>. American Journal of Medical Genetics Part A. https://doi.org/10.1002/ajmg.a.62359

Source records

crossref · retrieved 2026-09-26T18:13:35.556Z