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Characterization of a Familial Goldenhar Syndrome Case Using Whole-Exome Sequencing — Europe PMC PMID:41898833

Source: Europe PMC (en)
Original: https://europepmc.org/article/MED/41898833
DOI: 10.3390/genes17030299
License (as archived): solo-consultazione
Archived: 2026-11-05T12:38:54.089Z
SHA-256 of the archived text: 150653a0bbb8fb7fceaf2b69327195c328ac724b921dcddbcbeb8adc4025f153
Stable URL of this page: https://metraipolis.com/documento/dc_e449b05cd7cd

How to cite

Characterization of a Familial Goldenhar Syndrome Case Using Whole-Exome Sequencing — Europe PMC PMID:41898833 — Europe PMC (en), https://europepmc.org/article/MED/41898833 (solo-consultazione); archived copy: https://metraipolis.com/documento/dc_e449b05cd7cd (Metraipolis archive dc_e449b05cd7cd, sha256 150653a0bbb8fb7fceaf2b69327195c328ac724b921dcddbcbeb8adc4025f153)

BibTeX

@misc{dce449b05cd7cd,
  title = {Characterization of a Familial Goldenhar Syndrome Case Using Whole-Exome Sequencing — Europe PMC PMID:41898833},
  howpublished = {Europe PMC (en)},
  url = {https://europepmc.org/article/MED/41898833},
  note = {License solo-consultazione; archived copy https://metraipolis.com/documento/dc_e449b05cd7cd; sha256 150653a0bbb8fb7fceaf2b69327195c328ac724b921dcddbcbeb8adc4025f153},
  year = {2026}
}

Archived text

The text is not reproduced here: the archive holds it as solo-consultazione (consultation only, no republication). Read it at the original source: https://europepmc.org/article/MED/41898833. Agents can read the archived copy with the MCP tool read_document.