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The duplication 17p13.3 phenotype: analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes.
Curry CJ, Rosenfeld JA, Grant E, Gripp KW, Anderson C, Aylsworth AS, Saad TB, Chizhikov VV, Dybose G, Fagerberg C, Falco M, Fels C, Fichera M, Graakjaer J, Greco D, Hair J, Hopkins E, Huggins M, Ladda R, Li C, Moeschler J, Nowaczyk MJ, Ozmore JR, Reitano S, Romano C, Roos L, Schnur RE, Sell S, Suwannarat P, Svaneby D, Szybowska M, Tarnopolsky M, Tervo R, Tsai AC, Tucker M, Vallee S, Wheeler FC, Zand DJ, Barkovich AJ, Aradhya S, Shaffer LG, Dobyns WB. Curry CJ, et al. Among authors: fels c. Am J Med Genet A. 2013 Aug;161A(8):1833-52. doi: 10.1002/ajmg.a.35996. Epub 2013 Jun 27. Am J Med Genet A. 2013. PMID: 23813913 Free PMC article.
Neuropsychological sequelae of bacterial and viral meningitis.
Schmidt H, Heimann B, Djukic M, Mazurek C, Fels C, Wallesch CW, Nau R. Schmidt H, et al. Among authors: fels c. Brain. 2006 Feb;129(Pt 2):333-45. doi: 10.1093/brain/awh711. Epub 2005 Dec 19. Brain. 2006. PMID: 16364957
Moyamoya syndrome associated with hemolytic anemia due to Hb Alesha.
Brockmann K, Stolpe S, Fels C, Khan N, Kulozik AE, Pekrun A. Brockmann K, et al. Among authors: fels c. J Pediatr Hematol Oncol. 2005 Aug;27(8):436-40. doi: 10.1097/01.mph.0000175409.21342.ea. J Pediatr Hematol Oncol. 2005. PMID: 16096527
18 results