Connection
John Carroll to Polymorphism, Single Nucleotide
This is a "connection" page, showing publications John Carroll has written about Polymorphism, Single Nucleotide.
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0.135 |
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Mulkey SB, Ben-Zeev B, Nicolai J, Carroll JL, Gr?nborg S, Jiang YH, Joshi N, Kelly M, Koolen DA, Mikati MA, Park K, Pearl PL, Scheffer IE, Spillmann RC, Taglialatela M, Vieker S, Weckhuysen S, Cooper EC, Cilio MR. Neonatal nonepileptic myoclonus is a prominent clinical feature of KCNQ2 gain-of-function variants R201C and R201H. Epilepsia. 2017 03; 58(3):436-445.
Score: 0.117
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Jambhekar SK, Carroll JL, Keiles S. Report of two patients with associated conditions in addition to cystic fibrosis. J Cyst Fibros. 2010 Jul; 9(4):269-71.
Score: 0.018