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Surrey, Lea F, MacFarland, Suzanne P, Chang, Fengqi, Cao, Kajia, Rathi, Komal S, Akgumus, Gozde T, Gallo, Daniel, Lin, Fumin, Gleason, Adam, Raman, Pichai, Aplenc, Richard, Bagatell, Rochelle, Minturn, Jane, Mosse, Yael, Santi, Mariarita, Tasian, Sarah K, Waanders, Angela J, Sarmady, Mahdi, Maris, John M, Hunger, Stephen P, Li, Marilyn M
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Published in Genome medicine (28.05.2019)
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PCDH19-related epilepsy in a male with Klinefelter syndrome: Additional evidence supporting PCDH19 cellular interference disease mechanism
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Published in Epilepsy research (01.09.2018)
Published in Epilepsy research (01.09.2018)
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Evolution of histomorphologic, cytogenetic, and genetic abnormalities in an untreated patient with MIRAGE syndrome
Rentas, Stefan, Pillai, Vinodh, Wertheim, Gerald B., Akgumus, Gozde T., Nichols, Kim E., Deardorff, Matthew A., Conlin, Laura K., Li, Marilyn M., Olson, Timothy S., Luo, Minjie
Published in Cancer genetics (01.07.2020)
Published in Cancer genetics (01.07.2020)
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10. Comprehensive genomic characterization of pediatric B-ALL
Luo, Minjie, Lin, Fumin, Zhao, Xiaonan, Tang, Junxia, Akgumus, Gozde T., Gallo, Daniel J., Romasko, Edward, Gleason, Adam G., Surrey, Lea F., Wertheim, Gerald, Li, Marilyn M.
Published in Cancer genetics (01.10.2018)
Published in Cancer genetics (01.10.2018)
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