Considering Multiple Acyl-CoA Dehydrogenase Deficiency (MADD) in Prenatal Genetic Assessment of Cystic Renal Anomalies.

Luke ND, James LS, Beck MM, Navaneethan PR, Aaron R, Danda S

Open source

DOI
10.1002/pd.70254
Published
2026 Sep 26
Container
Prenatal diagnosis
Publisher
Not recorded
Open access
unknown

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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

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