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Year | Number of Results |
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1997 | 1 |
2002 | 1 |
2017 | 1 |
2022 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 8364
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Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndrome.
Am J Hum Genet. 2022 Apr 7;109(4):750-758. doi: 10.1016/j.ajhg.2022.02.003. Epub 2022 Feb 23.
Am J Hum Genet. 2022.
PMID: 35202563
Free PMC article.
Germline mutations affecting the histone H4 core cause a developmental syndrome by altering DNA damage response and cell cycle control.
Tessadori F, Giltay JC, Hurst JA, Massink MP, Duran K, Vos HR, van Es RM; Deciphering Developmental Disorders Study; Scott RH, van Gassen KLI, Bakkers J, van Haaften G.
Tessadori F, et al.
Nat Genet. 2017 Nov;49(11):1642-1646. doi: 10.1038/ng.3956. Epub 2017 Sep 18.
Nat Genet. 2017.
PMID: 28920961
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The human and mouse replication-dependent histone genes.
Marzluff WF, Gongidi P, Woods KR, Jin J, Maltais LJ.
Marzluff WF, et al.
Genomics. 2002 Nov;80(5):487-98.
Genomics. 2002.
PMID: 12408966
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Human histone gene organization: nonregular arrangement within a large cluster.
Albig W, Kioschis P, Poustka A, Meergans K, Doenecke D.
Albig W, et al.
Genomics. 1997 Mar 1;40(2):314-22. doi: 10.1006/geno.1996.4592.
Genomics. 1997.
PMID: 9119399
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