OMIM/309590[Secondary Source ID] - Search Results

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Human diseases with underlying defects in chromatin structure and modification.

Hendrich B, Bickmore W. Hendrich B, et al. Hum Mol Genet. 2001 Oct 1;10(20):2233-42. doi: 10.1093/hmg/10.20.2233. Hum Mol Genet. 2001. PMID: 11673406 Review.

Expanding phenotype of XNP mutations: mild to moderate mental retardation.

Yntema HG, Poppelaars FA, Derksen E, Oudakker AR, van Roosmalen T, Jacobs A, Obbema H, Brunner HG, Hamel BC, van Bokhoven H. Yntema HG, et al. Am J Med Genet. 2002 Jul 1;110(3):243-7. doi: 10.1002/ajmg.10446. Am J Med Genet. 2002. PMID: 12116232

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