Connection
Curtis Coughlin II to Polymorphism, Single Nucleotide
This is a "connection" page, showing publications Curtis Coughlin II has written about Polymorphism, Single Nucleotide.
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0.054 |
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Sampson MG, Coughlin CR, Kaplan P, Conlin LK, Meyers KE, Zackai EH, Spinner NB, Copelovitch L. Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung disease. Am J Med Genet A. 2010 Oct; 152A(10):2618-22.
Score: 0.054