Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Editorial
. 2022 Oct;30(10):1095-1096.
doi: 10.1038/s41431-022-01188-6.

Happy 30th birthday to the European Journal of Human Genetics!

Affiliations
Editorial

Happy 30th birthday to the European Journal of Human Genetics!

Alisdair McNeill. Eur J Hum Genet. 2022 Oct.
No abstract available

PubMed Disclaimer

Conflict of interest statement

The author declares no competing interests.

Similar articles

References

    1. Corbie R, Campbell T, Darwent L, Rudge P, Collinge J, Mead S. Estimation of the number of inherited prion disease mutation carriers in the UK. Eur J Hum Genet. 2022. 10.1038/s41431-022-01132-8. - PMC - PubMed
    1. Ewans LJ, Minoche AE, Schofield D, Shrestha R, Puttick C, Zhu Y, et al. Whole exome and genome sequencing in mendelian disorders: a diagnostic and health economic analysis. Eur J Hum Genet. 2022. 10.1038/s41431-022-01162-2. - PMC - PubMed
    1. Eyries M, Ariste O, Legrand G, Basset N, Guillerm E, Perrier A, et al. Detection of a pathogenic Alu element insertion in PALB2 gene from targeted NGS diagnostic data. Eur J Hum Genet. 2022. 10.1038/s41431-022-01064-3. - PMC - PubMed
    1. Yıldız Bölükbaşı E, Karolak JA, Szafranski P, Gambin T, Matsika A, McManus S, et al. Variable expressivity in a four-generation ACDMPV family with a non-coding hypermorphic SNV in trans to the frameshifting FOXF1 variant. Eur J Hum Genet. 2022. 10.1038/s41431-022-01159-x. - PMC - PubMed
    1. Carter S, Fellows BJ, Gibson K, Bicknell LS. Extending the PAX1 spectrum: a dominantly inherited variant causes oculo-auriculo-vertebral syndrome. Eur J Hum Genet. 2022. 10.1038/s41431-022-01154-2. - PMC - PubMed

Publication types