 Connection
Shawn McCandless to Polymorphism, Single Nucleotide
This is a "connection" page, showing publications Shawn McCandless has written about Polymorphism, Single Nucleotide.
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0.280 |
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Tarini BA, Konczal LL, Goldenberg AJ, Goldman EB, McCandless SE. The perils of SNP microarray testing: uncovering unexpected consanguinity. Pediatr Neurol. 2013 Jul; 49(1):50-3.
Score: 0.259
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Al-Kateb H, Hahn A, Gastier-Foster JM, Jeng L, McCandless SE, Curtis CA. Molecular characterization of a novel, de novo, cryptic interstitial deletion on 19p13.3 in a child with a cutis aplasia and multiple congenital anomalies. Am J Med Genet A. 2010 Dec; 152A(12):3148-53.
Score: 0.014
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Andresen BS, Dobrowolski SF, O'Reilly L, Muenzer J, McCandless SE, Frazier DM, Udvari S, Bross P, Knudsen I, Banas R, Chace DH, Engel P, Naylor EW, Gregersen N. Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency. Am J Hum Genet. 2001 Jun; 68(6):1408-18.
Score: 0.007
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Connection Strength
The connection strength for concepts is the sum of the scores for each matching publication.
Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
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