Prenatally Detected Maternally Inherited Partial Duplication of 11p15.5 ICR1 Results in Phenotypes Overlapping Russell‐Silver Syndrome in Infancy
- DOI
- 10.1002/pd.6832
- Published
- 2025-06-12
- Container
- Prenatal Diagnosis
- Publisher
- Wiley
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1002/pd.6832,
title = {Prenatally Detected Maternally Inherited Partial Duplication of 11p15.5 ICR1 Results in Phenotypes Overlapping Russell‐Silver Syndrome in Infancy},
author = {Amanda Thomas‐Wilson and Mythily Ganapathi and Nina Harkavy and Corbin Schwanke and Jessica Giordano and Abdallah F. Elias and Ronald J. Wapner and Vaidehi Jobanputra},
year = {2025},
journal = {Prenatal Diagnosis},
doi = {10.1002/pd.6832},
url = {https://doi.org/10.1002/pd.6832}
}RIS
TY - JOUR TI - Prenatally Detected Maternally Inherited Partial Duplication of 11p15.5 ICR1 Results in Phenotypes Overlapping Russell‐Silver Syndrome in Infancy AU - Amanda Thomas‐Wilson AU - Mythily Ganapathi AU - Nina Harkavy AU - Corbin Schwanke AU - Jessica Giordano AU - Abdallah F. Elias AU - Ronald J. Wapner AU - Vaidehi Jobanputra PY - 2025 JO - Prenatal Diagnosis DO - 10.1002/pd.6832 UR - https://doi.org/10.1002/pd.6832 ER -
APA
Thomas‐Wilson, A., Ganapathi, M., Harkavy, N., Schwanke, C., Giordano, J., Elias, A. F., Wapner, R. J., & Jobanputra, V. (2025). Prenatally Detected Maternally Inherited Partial Duplication of 11p15.5 ICR1 Results in Phenotypes Overlapping Russell‐Silver Syndrome in Infancy. Prenatal Diagnosis. https://doi.org/10.1002/pd.6832
Source records
- crossref · retrieved 2026-09-25T21:54:07.195Z