Fond farewell to clinical utility gene cards
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
https://www.nature.com/articles/s41431-021-00957-z.pdf
Reference9 articles.
1. Aamir A, Kuht HJ, Grønskov K, Brooks BP, Thomas MG. Clinical utility gene card for oculocutaneous (OCA) and ocular albinism (OA)—an update. Eur J Hum Genet. 2021. https://doi.org/10.1038/s41431-021-00809-w.
2. Dawar B, Kuht HJ, Han J, Maconachie GDE, Thomas MG. Clinical utility gene card for FRMD7-related infantile nystagmus. Eur J Hum Genet. 2021. https://doi.org/10.1038/s41431-021-00826-9.
3. Pollard S, Weymann D, Dunne J, Mayanloo F, Buckell J, Buchanan J, et al. Toward the diagnosis of rare childhood genetic diseases: what do parents value most? Eur J Hum Genet. 2021. https://doi.org/10.1038/s41431-021-00882-1.
4. Hallinan D, Bernier A, Cambon-Thomsen A, Crawley FP, Dimitrova D, Medeiros CB, et al. International transfers of personal data for health research following Schrems II: a problem in need of a solution. Eur J Hum Genet. 2021. https://doi.org/10.1038/s41431-021-00893-y.
5. Hay E, Wilson LC, Hoskins B, Samuels M, Munot P, Rahman S. Biallelic P4HTM variants associated with HIDEA syndrome and mitochondrial respiratory chain complex I deficiency. Eur J Hum Genet. 2021. https://doi.org/10.1038/s41431-021-00932-8.
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