Considering Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in Prenatal Genetic Assessment of Cystic Renal Anomalies.
- DOI
- 10.1002/pd.70254
- Published
- 2026 Sep 26
- Container
- Prenatal diagnosis
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1002/pd.70254,
title = {Considering Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in Prenatal Genetic Assessment of Cystic Renal Anomalies.},
author = {Luke ND and James LS and Beck MM and Navaneethan PR and Aaron R and Danda S},
year = {2026},
journal = {Prenatal diagnosis},
doi = {10.1002/pd.70254},
url = {https://doi.org/10.1002/pd.70254}
}RIS
TY - JOUR TI - Considering Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in Prenatal Genetic Assessment of Cystic Renal Anomalies. AU - Luke ND AU - James LS AU - Beck MM AU - Navaneethan PR AU - Aaron R AU - Danda S PY - 2026 JO - Prenatal diagnosis DO - 10.1002/pd.70254 UR - https://doi.org/10.1002/pd.70254 ER -
APA
ND, L., LS, J., MM, B., PR, N., R, A., & S, D. (2026). Considering Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in Prenatal Genetic Assessment of Cystic Renal Anomalies.. Prenatal diagnosis. https://doi.org/10.1002/pd.70254
Source records
- pubmed · retrieved 2026-09-27T11:43:40.592Z