Author/Creator: Farwell, Kelly D. - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Farwell, Kelly D.

1. Diagnostic Exome Sequencing Identifies a Novel Gene, EMILIN1, Associated with Autosomal‐Dominant Hereditary Connective Tissue Disease. Issue 1 (4th November 2015)

Authors:: Capuano, Alessandra; Bucciotti, Francesco; Farwell, Kelly D.; Tippin Davis, Brigette; Mroske, Cameron; Hulick, Peter J.; Weissman, Scott M.; Gao, Qingshen; Spessotto, Paola; Colombatti, Alfonso; Doliana, Roberto
Journal:: Human mutation
Issue:: Volume 37:Issue 1(2016)
Page Start:: 84
Record Type:: Journal Article
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2. ELP2 is a novel gene implicated in neurodevelopmental disabilities. (2nd April 2015)

Authors:: Cohen, Julie S.; Srivastava, Siddharth; Farwell, Kelly D.; Lu, Hsiao‐Mei; Zeng, Wenqi; Lu, Hong; Chao, Elizabeth C.; Fatemi, Ali
Journal:: American journal of medical genetics
Issue:: Volume 167:Number 6(2015:Jun.)
Page Start:: 1391
Record Type:: Journal Article
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