Case Report: Concurrent maternal uniparental disomy-type Prader-Willi syndrome and X-linked G6PD deficiency-an area of focus on multi-gene screening for imprinting disorders.
- DOI
- 10.3389/fped.2026.1924208
- Published
- 2026
- Container
- Frontiers in pediatrics
- Publisher
- Not recorded
- Open access
- yes
Credibility signals
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Cite this work
BibTeX
@article{allodium:10.3389/fped.2026.1924208,
title = {Case Report: Concurrent maternal uniparental disomy-type Prader-Willi syndrome and X-linked G6PD deficiency-an area of focus on multi-gene screening for imprinting disorders.},
author = {Zhou Q and Yuan JM and Zou CC},
year = {2026},
journal = {Frontiers in pediatrics},
doi = {10.3389/fped.2026.1924208},
url = {https://doi.org/10.3389/fped.2026.1924208}
}RIS
TY - JOUR TI - Case Report: Concurrent maternal uniparental disomy-type Prader-Willi syndrome and X-linked G6PD deficiency-an area of focus on multi-gene screening for imprinting disorders. AU - Zhou Q AU - Yuan JM AU - Zou CC PY - 2026 JO - Frontiers in pediatrics DO - 10.3389/fped.2026.1924208 UR - https://doi.org/10.3389/fped.2026.1924208 ER -
APA
Q, Z., JM, Y., & CC, Z. (2026). Case Report: Concurrent maternal uniparental disomy-type Prader-Willi syndrome and X-linked G6PD deficiency-an area of focus on multi-gene screening for imprinting disorders.. Frontiers in pediatrics. https://doi.org/10.3389/fped.2026.1924208
Source records
- pubmed · retrieved 2026-11-10T09:58:58.865Z