Alberto Santiago-Cornier to Mutation
This is a "connection" page, showing publications Alberto Santiago-Cornier has written about Mutation.
Connection Strength
0.150
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Giampietro PF, Armstrong L, Stoddard A, Blank RD, Livingston J, Raggio CL, Rasmussen K, Pickart M, Lorier R, Turner A, Sund S, Sobrera N, Neptune E, Sweetser D, Santiago-Cornier A, Broeckel U. Whole exome sequencing identifies a POLRID mutation segregating in a father and two daughters with findings of Klippel-Feil and Treacher Collins syndromes. Am J Med Genet A. 2015 Jan; 167A(1):95-102.
Score: 0.088
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Cruz-Centeno N, Saenz-Maisonet JF, L?pez-Dones PM, Santiago-Cornier A, Ortiz-Justiniano VN. Mutations in COL1A1 and COL27A1 Associated with a Pectus Excavatum Phenotype in 2 Siblings with Osteogenesis Imperfecta. Am J Case Rep. 2022 May 18; 23:e935526.
Score: 0.037
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Vicary GW, Vergne Y, Santiago-Cornier A, Young LR, Roman J. Pulmonary Fibrosis in Hermansky-Pudlak Syndrome. Ann Am Thorac Soc. 2016 10; 13(10):1839-1846.
Score: 0.025