Prenatal and postnatal manifestations of WBP11-related disorder in Chinese patients: expanding the phenotypic and mutational spectrum.

Ma T, Liu J, Wang Y, Zhu H, Qin Y, Liu R, Yuan H, Ye B, Hua R, Li S, Xi H, Wang J, Li N

DOI: 10.1186/s40246-026-00966-3
Published: 2026 Apr 13
Container: Human genomics
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1186/s40246-026-00966-3,
  title = {Prenatal and postnatal manifestations of WBP11-related disorder in Chinese patients: expanding the phenotypic and mutational spectrum.},
  author = {Ma T and Liu J and Wang Y and Zhu H and Qin Y and Liu R and Yuan H and Ye B and Hua R and Li S and Xi H and Wang J and Li N},
  year = {2026},
  journal = {Human genomics},
  doi = {10.1186/s40246-026-00966-3},
  url = {https://doi.org/10.1186/s40246-026-00966-3}
}

RIS

TY  - JOUR
TI  - Prenatal and postnatal manifestations of WBP11-related disorder in Chinese patients: expanding the phenotypic and mutational spectrum.
AU  - Ma T
AU  - Liu J
AU  - Wang Y
AU  - Zhu H
AU  - Qin Y
AU  - Liu R
AU  - Yuan H
AU  - Ye B
AU  - Hua R
AU  - Li S
AU  - Xi H
AU  - Wang J
AU  - Li N
PY  - 2026
JO  - Human genomics
DO  - 10.1186/s40246-026-00966-3
UR  - https://doi.org/10.1186/s40246-026-00966-3
ER  -

APA

T, M., J, L., Y, W., H, Z., Y, Q., R, L., H, Y., B, Y., R, H., S, L., H, X., J, W., & N, L. (2026). Prenatal and postnatal manifestations of WBP11-related disorder in Chinese patients: expanding the phenotypic and mutational spectrum.. Human genomics. https://doi.org/10.1186/s40246-026-00966-3

Source records

pubmed · retrieved 2026-09-25T22:45:50.039Z