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5. Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study. Cardinale CJ; Li D; Tian L; Connolly JJ; March ME; Hou C; Wang F; Snyder J; Kim CE; Chiavacci RM; Sleiman PM; Burnham JM; Hakonarson H BMC Musculoskelet Disord; 2016 Nov; 17(1):462. PubMed ID: 27829420 [TBL] [Abstract][Full Text] [Related]
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