Leveraging Next-Generation Phenotyping in Dysmorphology to Support Variant Interpretation in Mowat-Wilson Syndrome.

Hsieh TC, Todd D, Warner T, Blankenship K, Saade D, Weiland H, Bhasin MA, Klinkhammer H, Li JM, Krawitz P, Chen WL, Luk HM, Tung ML, Chandra B

Open source

DOI: 10.1212/nxg.0000000000200384
Published: 2026 Aug
Container: Neurology. Genetics
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1212/nxg.0000000000200384,
  title = {Leveraging Next-Generation Phenotyping in Dysmorphology to Support Variant Interpretation in Mowat-Wilson Syndrome.},
  author = {Hsieh TC and Todd D and Warner T and Blankenship K and Saade D and Weiland H and Bhasin MA and Klinkhammer H and Li JM and Krawitz P and Chen WL and Luk HM and Tung ML and Chandra B},
  year = {2026},
  journal = {Neurology. Genetics},
  doi = {10.1212/nxg.0000000000200384},
  url = {https://doi.org/10.1212/nxg.0000000000200384}
}

RIS

TY  - JOUR
TI  - Leveraging Next-Generation Phenotyping in Dysmorphology to Support Variant Interpretation in Mowat-Wilson Syndrome.
AU  - Hsieh TC
AU  - Todd D
AU  - Warner T
AU  - Blankenship K
AU  - Saade D
AU  - Weiland H
AU  - Bhasin MA
AU  - Klinkhammer H
AU  - Li JM
AU  - Krawitz P
AU  - Chen WL
AU  - Luk HM
AU  - Tung ML
AU  - Chandra B
PY  - 2026
JO  - Neurology. Genetics
DO  - 10.1212/nxg.0000000000200384
UR  - https://doi.org/10.1212/nxg.0000000000200384
ER  -

APA

TC, H., D, T., T, W., K, B., D, S., H, W., MA, B., H, K., JM, L., P, K., WL, C., HM, L., ML, T., & B, C. (2026). Leveraging Next-Generation Phenotyping in Dysmorphology to Support Variant Interpretation in Mowat-Wilson Syndrome.. Neurology. Genetics. https://doi.org/10.1212/nxg.0000000000200384

Source records

pubmed · retrieved 2026-09-26T16:06:09.676Z