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Showing results 13 to 16 of 16 < previous

Preview	Issue Date	Title	Author(s)
	2015	Revealing missing human protein isoforms based on ab initio prediction, RNA-seq and proteomics	Hu, Z.; Scott, H.; Qin, G.; Zheng, G.; Chu, X.; Xie, L.; Adelson, D.; Oftedal, B.; Venugopal, P.; Babic, M.; Hahn, C.; Zhang, B.; Wang, X.; Li, N.; Wei, C.
	2020	RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML	Brown, A.L.; Arts, P.; Carmichael, C.L.; Babic, M.; Dobbins, J.; Chong, C.-E.; Schreiber, A.W.; Feng, J.; Phillips, K.; Wang, P.P.S.; Ha, T.; Homan, C.C.; King-Smith, S.L.; Rawlings, L.; Vakulin, C.; Dubowsky, A.; Burdett, J.; Moore, S.; McKavanagh, G.; Henry, D.; et al.
	2021	Targeted gene panels identify a high frequency of pathogenic germline variants in patients diagnosed with a hematological malignancy and at least one other independent cancer	Singhal, D.; Hahn, C.N.; Feurstein, S.; Wee, L.Y.A.; Moma, L.; Kutyna, M.M.; Chhetri, R.; Eshraghi, L.; Schreiber, A.W.; Feng, J.; Wang, P.P.-S.; Babic, M.; Parker, W.T.; Gao, S.; Moore, S.; Das, S.; Thomas, D.; Pattnaik, S.; Brown, A.L.; D'Andrea, R.J.; et al.
	2020	Two monogenic disorders masquerading as one: severe congenital neutropenia with monocytosis and non-syndromic sensorineural hearing loss	Venugopal, P.; Gagliardi, L.; Forsyth, C.; Feng, J.; Phillips, K.; Babic, M.; Poplawski, N.K.; Rienhoff, H.Y.; Schreiber, A.W.; Hahn, C.N.; Brown, A.L.; Scott, H.S.

Showing results 13 to 16 of 16 < previous