Comprehensive Assessment of the KDM2B-Associated Neurodevelopmental Disorder and the 12q24.31 Microdeletion Syndrome.

van Oirsouw ASE, Hsieh TC, Koetsier M, Alali A, Albuainain F, Bacchelli E, Barakat TS, Capri Y, Chantot-Bastaraud S, Capra V, Carere DA, Clement E, Elkhateeb N, Franchi M, Li JM, Matthews N, McNiven V, Mehta SG, Nakamura M, Phornphutkul C, Revencu N, Scala M, Shallow N, Stefanich J, Viggiano M, Visconti P, Walker S, Zara F, Alders M, Koeleman BPC, Oegema R

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DOI: 10.1111/cge.70169
Published: 2026 Aug
Container: Clinical genetics
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1111/cge.70169,
  title = {Comprehensive Assessment of the KDM2B-Associated Neurodevelopmental Disorder and the 12q24.31 Microdeletion Syndrome.},
  author = {van Oirsouw ASE and Hsieh TC and Koetsier M and Alali A and Albuainain F and Bacchelli E and Barakat TS and Capri Y and Chantot-Bastaraud S and Capra V and Carere DA and Clement E and Elkhateeb N and Franchi M and Li JM and Matthews N and McNiven V and Mehta SG and Nakamura M and Phornphutkul C and Revencu N and Scala M and Shallow N and Stefanich J and Viggiano M and Visconti P and Walker S and Zara F and Alders M and Koeleman BPC and Oegema R},
  year = {2026},
  journal = {Clinical genetics},
  doi = {10.1111/cge.70169},
  url = {https://doi.org/10.1111/cge.70169}
}

RIS

TY  - JOUR
TI  - Comprehensive Assessment of the KDM2B-Associated Neurodevelopmental Disorder and the 12q24.31 Microdeletion Syndrome.
AU  - van Oirsouw ASE
AU  - Hsieh TC
AU  - Koetsier M
AU  - Alali A
AU  - Albuainain F
AU  - Bacchelli E
AU  - Barakat TS
AU  - Capri Y
AU  - Chantot-Bastaraud S
AU  - Capra V
AU  - Carere DA
AU  - Clement E
AU  - Elkhateeb N
AU  - Franchi M
AU  - Li JM
AU  - Matthews N
AU  - McNiven V
AU  - Mehta SG
AU  - Nakamura M
AU  - Phornphutkul C
AU  - Revencu N
AU  - Scala M
AU  - Shallow N
AU  - Stefanich J
AU  - Viggiano M
AU  - Visconti P
AU  - Walker S
AU  - Zara F
AU  - Alders M
AU  - Koeleman BPC
AU  - Oegema R
PY  - 2026
JO  - Clinical genetics
DO  - 10.1111/cge.70169
UR  - https://doi.org/10.1111/cge.70169
ER  -

APA

ASE, V. O., TC, H., M, K., A, A., F, A., E, B., TS, B., Y, C., S, C., V, C., DA, C., E, C., N, E., M, F., JM, L., N, M., V, M., SG, M., M, N., C, P., N, R., M, S., N, S., J, S., M, V., P, V., S, W., F, Z., M, A., BPC, K., & R, O. (2026). Comprehensive Assessment of the KDM2B-Associated Neurodevelopmental Disorder and the 12q24.31 Microdeletion Syndrome.. Clinical genetics. https://doi.org/10.1111/cge.70169

Source records

pubmed · retrieved 2026-09-24T22:44:14.586Z