A comprehensive approach to users from a Brazilian clinical genetics service: an observational study.

de Francisco DD, Silva IMW, Steiner CE, Gil-da-Silva-Lopes VL

Open source

DOI: 10.1186/s13023-026-04390-7
Published: 2026 May 20
Container: Orphanet journal of rare diseases
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1186/s13023-026-04390-7,
  title = {A comprehensive approach to users from a Brazilian clinical genetics service: an observational study.},
  author = {de Francisco DD and Silva IMW and Steiner CE and Gil-da-Silva-Lopes VL},
  year = {2026},
  journal = {Orphanet journal of rare diseases},
  doi = {10.1186/s13023-026-04390-7},
  url = {https://doi.org/10.1186/s13023-026-04390-7}
}

RIS

TY  - JOUR
TI  - A comprehensive approach to users from a Brazilian clinical genetics service: an observational study.
AU  - de Francisco DD
AU  - Silva IMW
AU  - Steiner CE
AU  - Gil-da-Silva-Lopes VL
PY  - 2026
JO  - Orphanet journal of rare diseases
DO  - 10.1186/s13023-026-04390-7
UR  - https://doi.org/10.1186/s13023-026-04390-7
ER  -

APA

DD, D. F., IMW, S., CE, S., & VL, G. (2026). A comprehensive approach to users from a Brazilian clinical genetics service: an observational study.. Orphanet journal of rare diseases. https://doi.org/10.1186/s13023-026-04390-7

Source records

pubmed · retrieved 2026-09-26T09:45:29.045Z
europe-pmc · retrieved 2026-09-26T09:45:29.058Z
doaj · retrieved 2026-09-26T09:45:29.044Z