William Dobyns to Chromosomes, Human, Pair 14
This is a "connection" page, showing publications William Dobyns has written about Chromosomes, Human, Pair 14.
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The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis. J Med Genet. 2011 Jun; 48(6):396-406.
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