Further delineation of Malan syndrome.
- DOI
- 10.1002/humu.23563
- Published
- 2018 Sep
- Container
- Human mutation
- Publisher
- Not recorded
- Open access
- yes
Credibility signals
limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
Show all credibility signals
- cautionDOI registered: No matching Crossref record was present in this response.
- cautionDOI resolves: No matching Crossref record was present in this response.
- 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.
- supportingOpen access status: Normalized open-access status: open.
- 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.
- cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty.
Cite this work
BibTeX
@article{allodium:10.1002/humu.23563,
title = {Further delineation of Malan syndrome.},
author = {Priolo M and Schanze D and Tatton-Brown K and Mulder PA and Tenorio J and Kooblall K and Acero IH and Alkuraya FS and Arias P and Bernardini L and Bijlsma EK and Cole T and Coubes C and Dapia I and Davies S and Di Donato N and Elcioglu NH and Fahrner JA and Foster A and González NG and Huber I and Iascone M and Kaiser AS and Kamath A and Liebelt J and Lynch SA and Maas SM and Mammì C and Mathijssen IB and McKee S and Menke LA and Mirzaa GM and Montgomery T and Neubauer D and Neumann TE and Pintomalli L and Pisanti MA and Plomp AS and Price S and Salter C and Santos-Simarro F and Sarda P and Segovia M and Shaw-Smith C and Smithson S and Suri M and Valdez RM and Van Haeringen A and Van Hagen JM and Zollino M and Lapunzina P and Thakker RV and Zenker M and Hennekam RC},
year = {2018},
journal = {Human mutation},
doi = {10.1002/humu.23563},
url = {https://doi.org/10.1002/humu.23563}
}RIS
TY - JOUR TI - Further delineation of Malan syndrome. AU - Priolo M AU - Schanze D AU - Tatton-Brown K AU - Mulder PA AU - Tenorio J AU - Kooblall K AU - Acero IH AU - Alkuraya FS AU - Arias P AU - Bernardini L AU - Bijlsma EK AU - Cole T AU - Coubes C AU - Dapia I AU - Davies S AU - Di Donato N AU - Elcioglu NH AU - Fahrner JA AU - Foster A AU - González NG AU - Huber I AU - Iascone M AU - Kaiser AS AU - Kamath A AU - Liebelt J AU - Lynch SA AU - Maas SM AU - Mammì C AU - Mathijssen IB AU - McKee S AU - Menke LA AU - Mirzaa GM AU - Montgomery T AU - Neubauer D AU - Neumann TE AU - Pintomalli L AU - Pisanti MA AU - Plomp AS AU - Price S AU - Salter C AU - Santos-Simarro F AU - Sarda P AU - Segovia M AU - Shaw-Smith C AU - Smithson S AU - Suri M AU - Valdez RM AU - Van Haeringen A AU - Van Hagen JM AU - Zollino M AU - Lapunzina P AU - Thakker RV AU - Zenker M AU - Hennekam RC PY - 2018 JO - Human mutation DO - 10.1002/humu.23563 UR - https://doi.org/10.1002/humu.23563 ER -
APA
M, P., D, S., K, T., PA, M., J, T., K, K., IH, A., FS, A., P, A., L, B., EK, B., T, C., C, C., I, D., S, D., N, D. D., NH, E., JA, F., A, F., NG, G., I, H., M, I., AS, K., A, K., J, L., SA, L., SM, M., C, M., IB, M., S, M., LA, M., GM, M., T, M., D, N., TE, N., L, P., MA, P., AS, P., S, P., C, S., F, S., P, S., M, S., C, S., S, S., M, S., RM, V., A, V. H., JM, V. H., M, Z., P, L., RV, T., M, Z., & RC, H. (2018). Further delineation of Malan syndrome.. Human mutation. https://doi.org/10.1002/humu.23563
Source records
- pubmed · retrieved 2026-09-26T15:07:53.245Z