de Greef, Jessica C <br/><br/>
Smchd1 haploinsufficiency exacerbates the phenotype of a transgenic FSHD1 mouse model.  [electronic resource] 

 -  Human molecular genetics  02 2018 
 - 716-731 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2083 
<br/><br/><label>Standard No.: </label>10.1093/hmg/ddx437  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Blotting, Western<br/>Cells, Cultured<br/>Chromosomal Proteins, Non-Histone--genetics<br/>DNA Methylation--genetics<br/>Fibroblasts--metabolism<br/>Flow Cytometry<br/>Haploinsufficiency--genetics<br/>Homeodomain Proteins--genetics<br/>Humans<br/>Keratinocytes--metabolism<br/>Mice<br/>Mice, Transgenic<br/>Muscle, Skeletal--metabolism<br/>Muscular Dystrophy, Facioscapulohumeral--genetics<br/>Phenotype<br/>Reverse Transcriptase Polymerase Chain Reaction<br/>Skin<br/>Thymocytes