These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. When enough is enough: genetic diseases associated with transcriptional derepression. Gabellini D; Green MR; Tupler R Curr Opin Genet Dev; 2004 Jun; 14(3):301-7. PubMed ID: 15172674 [TBL] [Abstract][Full Text] [Related]
6. Epigenetic mechanisms of facioscapulohumeral muscular dystrophy. de Greef JC; Frants RR; van der Maarel SM Mutat Res; 2008 Dec; 647(1-2):94-102. PubMed ID: 18723032 [TBL] [Abstract][Full Text] [Related]
7. An epigenetic basis for genetic anticipation in facioscapulohumeral muscular dystrophy type 1. Zheng F; Qiu L; Chen L; Zheng Y; He Q; Lin X; Lin M; Lin Y; Fu Y; Wang N; Wang Z Brain; 2023 Dec; 146(12):e107-e110. PubMed ID: 37352893 [No Abstract] [Full Text] [Related]
8. Reply: An epigenetic basis for genetic anticipation in facioscapulohumeral muscular dystrophy type 1. Erdmann H; Scharf F; Hallermayr A; Barseghyan H; Walter MC; Holinski-Feder E; Schoser B; Abicht A Brain; 2023 Dec; 146(12):e111-e114. PubMed ID: 37348868 [No Abstract] [Full Text] [Related]
12. Case Studies on the Genetic and Clinical Diagnosis of Facioscapulohumeral Muscular Dystrophy. Hamel J; Tawil R Neurol Clin; 2020 Aug; 38(3):529-540. PubMed ID: 32703466 [TBL] [Abstract][Full Text] [Related]
13. The Epigenetic Regulator SMCHD1 in Development and Disease. Jansz N; Chen K; Murphy JM; Blewitt ME Trends Genet; 2017 Apr; 33(4):233-243. PubMed ID: 28222895 [TBL] [Abstract][Full Text] [Related]
14. Monosomy 18p is a risk factor for facioscapulohumeral dystrophy. Balog J; Goossens R; Lemmers RJLF; Straasheijm KR; van der Vliet PJ; Heuvel AVD; Cambieri C; Capet N; Feasson L; Manel V; Contet J; Kriek M; Donlin-Smith CM; Ruivenkamp CAL; Heard P; Tapscott SJ; Cody JD; Tawil R; Sacconi S; van der Maarel SM J Med Genet; 2018 Jul; 55(7):469-478. PubMed ID: 29563141 [TBL] [Abstract][Full Text] [Related]
15. Identification of Epigenetic Regulators of DUX4-fl for Targeted Therapy of Facioscapulohumeral Muscular Dystrophy. Himeda CL; Jones TI; Virbasius CM; Zhu LJ; Green MR; Jones PL Mol Ther; 2018 Jul; 26(7):1797-1807. PubMed ID: 29759937 [TBL] [Abstract][Full Text] [Related]
16. Digenic Inheritance in Rare Disorders and Mitochondrial Disease-Crossing the Frontier to a More Comprehensive Understanding of Etiology. Neuhofer CM; Prokisch H Int J Mol Sci; 2024 Apr; 25(9):. PubMed ID: 38731822 [TBL] [Abstract][Full Text] [Related]
19. Rapid and accurate diagnosis of facioscapulohumeral muscular dystrophy. Goto K; Nishino I; Hayashi YK Neuromuscul Disord; 2006 Apr; 16(4):256-61. PubMed ID: 16545566 [TBL] [Abstract][Full Text] [Related]
20. A hospital based epidemiological study of genetically determined muscle disease in south western Norway. Husebye SA; Rebne CB; Stokland AE; Sanaker PS; Bindoff LA Neuromuscul Disord; 2020 Mar; 30(3):181-185. PubMed ID: 32146000 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]