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Dive into the research topics of 'Erratum: TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities (The American Journal of Human Genetics (2013) 93(2) (197–210), (S0002929713002693), (10.1016/j.ajhg.2013.05.027))'. Together they form a unique fingerprint.- Sort by
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