Prenatal Diagnosis of Radio-Tartaglia Syndrome Caused by a Loss-of-Function Variant in SPEN in a Chinese Family.
- DOI
- 10.1002/jdn.70098
- Published
- 2026 Feb
- Container
- International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1002/jdn.70098,
title = {Prenatal Diagnosis of Radio-Tartaglia Syndrome Caused by a Loss-of-Function Variant in SPEN in a Chinese Family.},
author = {He Y and Gao L and Xu S and Li G and Han X and Hua R and Li S and Li N},
year = {2026},
journal = {International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience},
doi = {10.1002/jdn.70098},
url = {https://doi.org/10.1002/jdn.70098}
}RIS
TY - JOUR TI - Prenatal Diagnosis of Radio-Tartaglia Syndrome Caused by a Loss-of-Function Variant in SPEN in a Chinese Family. AU - He Y AU - Gao L AU - Xu S AU - Li G AU - Han X AU - Hua R AU - Li S AU - Li N PY - 2026 JO - International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience DO - 10.1002/jdn.70098 UR - https://doi.org/10.1002/jdn.70098 ER -
APA
Y, H., L, G., S, X., G, L., X, H., R, H., S, L., & N, L. (2026). Prenatal Diagnosis of Radio-Tartaglia Syndrome Caused by a Loss-of-Function Variant in SPEN in a Chinese Family.. International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience. https://doi.org/10.1002/jdn.70098
Source records
- pubmed · retrieved 2026-09-25T12:19:47.233Z