OMIM/242860[Secondary Source ID] - Search Results

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2003	2
2005	1
2025	0

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Perturbations of chromatin structure in human genetic disease: recent advances.

Bickmore WA, van der Maarel SM. Bickmore WA, et al. Hum Mol Genet. 2003 Oct 15;12 Spec No 2:R207-13. doi: 10.1093/hmg/ddg260. Epub 2003 Aug 5. Hum Mol Genet. 2003. PMID: 12915455 Review.

Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy.

van Overveld PG, Lemmers RJ, Sandkuijl LA, Enthoven L, Winokur ST, Bakels F, Padberg GW, van Ommen GJ, Frants RR, van der Maarel SM. van Overveld PG, et al. Nat Genet. 2003 Dec;35(4):315-7. doi: 10.1038/ng1262. Epub 2003 Nov 23. Nat Genet. 2003. PMID: 14634647

Non-skewed X-inactivation may cause mental retardation in a female carrier of X-linked alpha-thalassemia/mental retardation syndrome (ATR-X): X-inactivation study of nine female carriers of ATR-X.

Wada T, Sugie H, Fukushima Y, Saitoh S. Wada T, et al. Am J Med Genet A. 2005 Sep 15;138(1):18-20. doi: 10.1002/ajmg.a.30901. Am J Med Genet A. 2005. PMID: 16100724

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