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
. 2021 Jul;29(7):1037.
doi: 10.1038/s41431-021-00931-9.

Clinical genetics-it's polygenic

Affiliations
Editorial

Clinical genetics-it's polygenic

Alisdair McNeill. Eur J Hum Genet. 2021 Jul.
No abstract available

PubMed Disclaimer

Conflict of interest statement

Dr Alisdair McNeill is Editor-in-Chief of the European Journal of Human Genetics.

References

    1. Buelow M, Süßmuth D, Smith LD, Aryani O, Castiglioni C, Stenzel W et al. Novel bi-allelic variants expand the SPTBN4-related genetic and phenotypic spectrum. Eur J Hum Genet. 2021. 10.1038/s41431-021-00846-5 - PMC - PubMed
    1. Knapp KM, Jenkins DE, Sullivan R, Harms FL, von Elsner L, Ockeloen CW et al. MCM complex members MCM3 and MCM7 are associated with a phenotypic spectrum from Meier-Gorlin syndrome to lipodystrophy and adrenal insufficiency. Eur J Hum Genet. 2021. 10.1038/s41431-021-00839-4 - PMC - PubMed
    1. Runolfsdottir HL, Sayer JA, Indridason OS, Edvardsson VO, Jensson BO, Arnadottir GA et al. Allele frequency of variants reported to cause adenine phosphoribosyltransferase deficiency. Eur J Hum Genet. 2021. 10.1038/s41431-020-00805-6 - PMC - PubMed
    1. Angelini C, Goizet C, Said SA, Camu W, Depienne C, Heron B et al. Evidence of mosaicism in SPAST variant carriers in four French families. Eur J Hum Genet. 2021. 10.1038/s41431-021-00847-4 - PMC - PubMed
    1. Whitworth J, Casey RT, Smith PS, Giger O, Martin JE, Clark G et al. Familial wild-type gastrointestinal stromal tumour in association with germline truncating variants in both SDHA and PALB2. Eur J Hum Genet. 2021. 10.1038/s41431-021-00862-5 - PMC - PubMed

Publication types