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Year | Number of Results |
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2019 | 1 |
2020 | 1 |
2021 | 2 |
2022 | 1 |
2024 | 0 |
PubMed (cited) for id: 619503
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Recurrent de novo missense variants in GNB2 can cause syndromic intellectual disability.
J Med Genet. 2022 May;59(5):511-516. doi: 10.1136/jmedgenet-2020-107462. Epub 2021 Jun 28.
J Med Genet. 2022.
PMID: 34183358
Second patient with GNB2-related neurodevelopmental disease: Further evidence for a gene-disease association.
Lansdon LA, Fleming EA, Viso FD, Sullivan BR, Saunders CJ.
Lansdon LA, et al.
Eur J Med Genet. 2021 Jul;64(7):104243. doi: 10.1016/j.ejmg.2021.104243. Epub 2021 May 7.
Eur J Med Genet. 2021.
PMID: 33971351
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Exome reports A de novo GNB2 variant associated with global developmental delay, intellectual disability, and dysmorphic features.
Fukuda T, Hiraide T, Yamoto K, Nakashima M, Kawai T, Yanagi K, Ogata T, Saitsu H.
Fukuda T, et al.
Eur J Med Genet. 2020 Apr;63(4):103804. doi: 10.1016/j.ejmg.2019.103804. Epub 2019 Nov 4.
Eur J Med Genet. 2020.
PMID: 31698099
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