Rare phenotypic spectrum of 17β-hydroxysteroid dehydrogenase 3 deficiency: case series from infancy to adolescence
- DOI
- 10.1515/jpem-2025-0549
- Published
- 2026-01-26
- Container
- Journal of Pediatric Endocrinology and Metabolism
- Publisher
- Walter de Gruyter GmbH
- Open access
- unknown
Credibility signals
uncertain Score 64/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
Show all credibility signals
- supportingDOI registered: A matching record was returned by Crossref.
- supportingDOI resolves: A matching record was returned by Crossref.
- not scoredDirectory of Open Access Journals: No matching DOAJ record was present in this response. No allow-list match; this is not evidence of low credibility.
- not scoredMEDLINE indexed: Not checked or no result supplied; no credibility inference made.
- not scoredOpenAlex core source: Not checked or no result supplied; no credibility inference made.
- not scoredKnown publisher allow-list: Not checked or no result supplied; no credibility inference made.
- not scoredROR affiliation: Not checked or no result supplied; no credibility inference made.
- not scoredRetraction Watch retraction: No retraction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch expression of concern: No expression of concern notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch correction: No correction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredRetraction Watch reinstatement: No reinstatement notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete.
- not scoredOpen access status: Not checked or no result supplied; no credibility inference made.
- not scoredPublication license: Not checked or no result supplied; no credibility inference made.
- not scoredPublication version: A publication version was supplied but is not scored.
- supportingMetadata completeness: All 6 scored descriptive metadata groups are present.
Cite this work
BibTeX
@article{allodium:10.1515/jpem-2025-0549,
title = {Rare phenotypic spectrum of 17β-hydroxysteroid dehydrogenase 3 deficiency: case series from infancy to adolescence},
author = {Subbiah Sridhar and Aravind Kumar Muthu and Sreenivasan Palaniappan and Kuppusamy Nandini and Aravindan Chandrasekaran and Rani Kalavathy},
year = {2026},
journal = {Journal of Pediatric Endocrinology and Metabolism},
doi = {10.1515/jpem-2025-0549},
url = {https://doi.org/10.1515/jpem-2025-0549}
}RIS
TY - JOUR TI - Rare phenotypic spectrum of 17β-hydroxysteroid dehydrogenase 3 deficiency: case series from infancy to adolescence AU - Subbiah Sridhar AU - Aravind Kumar Muthu AU - Sreenivasan Palaniappan AU - Kuppusamy Nandini AU - Aravindan Chandrasekaran AU - Rani Kalavathy PY - 2026 JO - Journal of Pediatric Endocrinology and Metabolism DO - 10.1515/jpem-2025-0549 UR - https://doi.org/10.1515/jpem-2025-0549 ER -
APA
Sridhar, S., Muthu, A. K., Palaniappan, S., Nandini, K., Chandrasekaran, A., & Kalavathy, R. (2026). Rare phenotypic spectrum of 17β-hydroxysteroid dehydrogenase 3 deficiency: case series from infancy to adolescence. Journal of Pediatric Endocrinology and Metabolism. https://doi.org/10.1515/jpem-2025-0549
Source records
- crossref · retrieved 2026-09-26T16:44:20.413Z