Dimensional phenotype measurement in children with rare genetic conditions: new insights into the aetiology of neurodevelopmental and psychiatric disorders

SJRA Chawner, LC Chetcuti, EK Spackman, M Uljarevic

Open source

DOI: 10.3389/fpsyt.2026.1602131
Published: 2026-04-13
Container: Frontiers in Psychiatry
Publisher: Frontiers Media SA
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.3389/fpsyt.2026.1602131,
  title = {Dimensional phenotype measurement in children with rare genetic conditions: new insights into the aetiology of neurodevelopmental and psychiatric disorders},
  author = {SJRA Chawner and LC Chetcuti and EK Spackman and M Uljarevic},
  year = {2026},
  journal = {Frontiers in Psychiatry},
  doi = {10.3389/fpsyt.2026.1602131},
  url = {https://doi.org/10.3389/fpsyt.2026.1602131}
}

RIS

TY  - JOUR
TI  - Dimensional phenotype measurement in children with rare genetic conditions: new insights into the aetiology of neurodevelopmental and psychiatric disorders
AU  - SJRA Chawner
AU  - LC Chetcuti
AU  - EK Spackman
AU  - M Uljarevic
PY  - 2026
JO  - Frontiers in Psychiatry
DO  - 10.3389/fpsyt.2026.1602131
UR  - https://doi.org/10.3389/fpsyt.2026.1602131
ER  -

APA

Chawner, S., Chetcuti, L., Spackman, E., & Uljarevic, M. (2026). Dimensional phenotype measurement in children with rare genetic conditions: new insights into the aetiology of neurodevelopmental and psychiatric disorders. Frontiers in Psychiatry. https://doi.org/10.3389/fpsyt.2026.1602131

Source records

crossref · retrieved 2026-09-26T08:43:03.462Z