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Risk/MRD adapted GMALL trials in adult ALL.
Gökbuget N, Raff R, Brügge-Mann M, Flohr T, Scheuring U, Pfeifer H, Bartram CR, Kneba M, Hoelzer D. Gökbuget N, et al. Among authors: raff r. Ann Hematol. 2004;83 Suppl 1:S129-31. doi: 10.1007/s00277-004-0850-2. Ann Hematol. 2004. PMID: 15124705
Exome sequencing in large, multiplex bipolar disorder families from Cuba.
Maaser A, Forstner AJ, Strohmaier J, Hecker J, Ludwig KU, Sivalingam S, Streit F, Degenhardt F, Witt SH, Reinbold CS, Koller AC, Raff R, Heilmann-Heimbach S, Fischer SB; Bipolar Disorder Working Group of the Psychiatric Genomics Consortium; Herms S, Hoffmann P, Thiele H, Nürnberg P, Löhlein Fier H, Orozco-Díaz G, Carmenate-Naranjo D, Proenza-Barzaga N, Auburger GWJ, Andlauer TFM, Cichon S, Marcheco-Teruel B, Mors O, Rietschel M, Nöthen MM. Maaser A, et al. Among authors: raff r. PLoS One. 2018 Oct 31;13(10):e0205895. doi: 10.1371/journal.pone.0205895. eCollection 2018. PLoS One. 2018. PMID: 30379966 Free PMC article.
Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate.
Mangold E, Böhmer AC, Ishorst N, Hoebel AK, Gültepe P, Schuenke H, Klamt J, Hofmann A, Gölz L, Raff R, Tessmann P, Nowak S, Reutter H, Hemprich A, Kreusch T, Kramer FJ, Braumann B, Reich R, Schmidt G, Jäger A, Reiter R, Brosch S, Stavusis J, Ishida M, Seselgyte R, Moore GE, Nöthen MM, Borck G, Aldhorae KA, Lace B, Stanier P, Knapp M, Ludwig KU. Mangold E, et al. Among authors: raff r. Am J Hum Genet. 2016 Apr 7;98(4):755-62. doi: 10.1016/j.ajhg.2016.02.013. Epub 2016 Mar 24. Am J Hum Genet. 2016. PMID: 27018475 Free PMC article.
Congenital diaphragmatic hernia in a case of Cat eye syndrome.
Alsat EA, Reutter H, Bagci S, Kipfmueller F, Engels H, Raff R, Mangold E, Gembruch U, Geipel A, Müller A, Schaible T. Alsat EA, et al. Among authors: raff r. Clin Case Rep. 2018 Jul 23;6(9):1786-1790. doi: 10.1002/ccr3.1646. eCollection 2018 Sep. Clin Case Rep. 2018. PMID: 30214764 Free PMC article.
225 results