T. Conrad Gilliam to Syndrome
This is a "connection" page, showing publications T. Conrad Gilliam has written about Syndrome.
Connection Strength
0.028
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LGI1 mutations in autosomal dominant partial epilepsy with auditory features. Neurology. 2004 Apr 13; 62(7):1120-6.
Score: 0.014
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Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndrome. Cytogenet Genome Res. 2004; 107(1-2):68-76.
Score: 0.014