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Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.
Am J Hum Genet. 2020 Oct 1;107(4):727-742. doi: 10.1016/j.ajhg.2020.08.013. Epub 2020 Sep 4.
Am J Hum Genet. 2020.
PMID: 32891193
Free PMC article.
A candidate X-linked mental retardation gene is a component of a new family of histone deacetylase-containing complexes.
Hakimi MA, Dong Y, Lane WS, Speicher DW, Shiekhattar R.
Hakimi MA, et al.
J Biol Chem. 2003 Feb 28;278(9):7234-9. doi: 10.1074/jbc.M208992200. Epub 2002 Dec 18.
J Biol Chem. 2003.
PMID: 12493763
Free article.
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Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t(8;13)(p11;q12) myeloproliferative syndrome.
Reiter A, Sohal J, Kulkarni S, Chase A, Macdonald DH, Aguiar RC, Gonçalves C, Hernandez JM, Jennings BA, Goldman JM, Cross NC.
Reiter A, et al.
Blood. 1998 Sep 1;92(5):1735-42.
Blood. 1998.
PMID: 9716603
Free article.
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