Novel COCH mutation in a family with autosomal dominant late onset sensorineural hearing impairment and tinnitus von Gallant, Emily, BA, Francey, Lauren, MS, Fetting, Heather, BS, Kaur, Maninder, MS, Hakonarson, Hakon, MD, Clark, Dinah, MS, Devoto, Marcella, PhD, Krantz, Ian D., MD

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Abstract LB-11: PTEN modulates EGFRvIII-induced SHP2 phosphorylation and translocation to affect glioblastoma sensitivity to tyrosine kinase inhibitors (TKIs) von Kapoor, Gurpreet Singh, Zhan, Yi, Fetting, Heather, O'Rourke, Donald M.

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Abstract 2990: Molecular subtyping of glioblastoma based on isoform level network modeling von Pal, Sharmistha, Zhang, ZhongFa, Gupta, Ravi, Bi, Yingtao, Fetting, Heather Heather, O'Rourke, Donald M., Davuluri, Ramana V.

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Homozygosity for the V37I GJB2 mutation in fifteen probands with mild to moderate sensorineural hearing impairment: Further confirmation of pathogenicity and haplotype analysis in... von Gallant, Emily, Francey, Lauren, Tsai, Ellen A., Berman, Micah, Zhao, Yaru, Fetting, Heather, Kaur, Maninder, Deardorff, Matthew A., Wilkens, Alisha, Clark, Dinah, Hakonarson, Hakon, Rehm, Heidi L., Krantz, Ian D.

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Homozygosity for the V37I GJB 2 mutation in fifteen probands with mild to moderate sensorineural hearing impairment: Further confirmation of pathogenicity and haplotype analysis in... von Gallant, Emily, Francey, Lauren, Tsai, Ellen A., Berman, Micah, Zhao, Yaru, Fetting, Heather, Kaur, Maninder, Deardorff, Matthew A., Wilkens, Alisha, Clark, Dinah, Hakonarson, Hakon, Rehm, Heidi L., Krantz, Ian D.

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