Michael Zapadka to Polymorphism, Single Nucleotide
This is a "connection" page, showing publications Michael Zapadka has written about Polymorphism, Single Nucleotide.
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Shashi V, Francis A, Hooper SR, Kranz PG, Zapadka M, Schoch K, Ip E, Tandon N, Howard TD, Keshavan MS. Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms. Eur J Hum Genet. 2012 Oct; 20(10):1051-7.
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