Louise Wang, Heena Desai, Shefali S Verma, Anh Le, Ryan Hausler, Anurag Verma, Renae Judy, Abigail Doucette, Peter E Gabriel, Katherine L Nathanson, Scott M Damrauer, Danielle L Mowery, Marylyn D Ritchie, Rachel L Kember, Kara N Maxwell. Genet Med 2022
Times Cited: 2
Times Cited: 2
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Identification of Unique, Heterozygous Germline Mutation, STK11 (p.F354L), in a Child with an Encapsulated Follicular Variant of Papillary Thyroid Carcinoma within Six Months of Completing Treatment for Neuroblastoma.
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Ultra-rare mutation in long-range enhancer predisposes to thyroid carcinoma with high penetrance.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.