BOR and BO syndromes are allelic defects of EYA1.

Christophe Vincent, Vasiliki Kalatzis, Sonia Abdelhak, Hassan Chaïb, Sylvie Compain, J Helias, F Vaneecloo, Christine Petit

Open source

DOI: 10.1007/bf03405924
Published: 1997-04-08
Container: European Journal of Human Genetics
Publisher: Not recorded
Open access: no

Credibility signals

limited evidence Score 43/100 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. Source: Crossref; license: CC0 metadata
cautionDOI resolves: No matching Crossref record was present in this response. Source: Crossref; license: CC0 metadata
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. Source: DOAJ; license: CC0
not scoredMEDLINE indexed: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredOpenAlex core source: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredKnown publisher allow-list: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredROR affiliation: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredRetraction Watch retraction: No retraction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
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. Source: Retraction Watch; license: CC BY 4.0
not scoredRetraction Watch correction: No correction notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
not scoredRetraction Watch reinstatement: No reinstatement notice matched this DOI in the deployed snapshot. No matching event found; coverage may be incomplete. Source: Retraction Watch; license: CC BY 4.0
not scoredOpen access status: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredPublication license: Not checked or no result supplied; no credibility inference made. Source: No authority result supplied; license: Unknown
not scoredPublication version: A publication version was supplied but is not scored. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer

Cite this work

BibTeX

@article{allodium:10.1007/bf03405924,
  title = {BOR and BO syndromes are allelic defects of EYA1.},
  author = {Christophe Vincent and Vasiliki Kalatzis and Sonia Abdelhak and Hassan Chaïb and Sylvie Compain and J Helias and F Vaneecloo and Christine Petit},
  year = {1997},
  journal = {European Journal of Human Genetics},
  doi = {10.1007/bf03405924},
  url = {https://doi.org/10.1007/bf03405924}
}

RIS

TY  - JOUR
TI  - BOR and BO syndromes are allelic defects of EYA1.
AU  - Christophe Vincent
AU  - Vasiliki Kalatzis
AU  - Sonia Abdelhak
AU  - Hassan Chaïb
AU  - Sylvie Compain
AU  - J Helias
AU  - F Vaneecloo
AU  - Christine Petit
PY  - 1997
JO  - European Journal of Human Genetics
DO  - 10.1007/bf03405924
UR  - https://doi.org/10.1007/bf03405924
ER  -

APA

Vincent, C., Kalatzis, V., Abdelhak, S., Chaïb, H., Compain, S., Helias, J., Vaneecloo, F., & Petit, C. (1997). BOR and BO syndromes are allelic defects of EYA1.. European Journal of Human Genetics. https://doi.org/10.1007/bf03405924

Source records

hal · retrieved 2026-11-10T13:18:30.511Z