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References

1. Ayakannu T, Wordsworth S, Parveen S, Shehadeh Z, Moselhi M. Rare presentation of Trisomy 8 syndrome. J Obstet Gynaecol. 2008 Oct;28(7):748-9. doi:10.1080/01443610802462027.
2. de Die-Smulders CE, Engelen JJ, Schrander-Stumpel CT, Govaerts LC, de Vries B,Vles JS, Wagemans A, Schijns-Fleuren S, Gillessen-Kaesbach G, Fryns JP. Inversionduplication of the short arm of chromosome 8: clinical data on seven patients andreview of the literature. Am J Med Genet. 1995 Nov 20;59(3):369-74. Review.
3. Feenstra I, van Ravenswaaij CM, van der Knaap MS, Willemsen MA. Neuroimagingin nine patients with inversion duplication of the short arm of chromosome 8.Neuropediatrics. 2006 Apr;37(2):83-7.
4. Gilbert F. Chromosome 8. Genet Test. 2001 Winter;5(4):345-54.
5. Golzio C, Guirchoun J, Ozilou C, Thomas S, Goudefroye G, Morichon-Delvallez N,Vekemans M, Attié-Bitach T, Etchevers HC. Cytogenetic and histological featuresof a human embryo with homogeneous chromosome 8 trisomy. Prenat Diagn. 2006Dec;26(13):1201-5.
6. Graw SL, Sample T, Bleskan J, Sujansky E, Patterson D. Cloning, sequencing,and analysis of inv8 chromosome breakpoints associated with recombinant 8syndrome. Am J Hum Genet. 2000 Mar;66(3):1138-44.
7. Hulley BJ, Hummel M, Cook LL, Boyd BK, Wenger SL. Trisomy 8 mosaicism:selective growth advantage of normal cells vs. growth disadvantage of trisomy 8cells. Am J Med Genet A. 2003 Jan 15;116A(2):144-6.
8. Jackson CC, Medeiros LJ, Miranda RN. 8p11 myeloproliferative syndrome: areview. Hum Pathol. 2010 Apr;41(4):461-76. doi: 10.1016/j.humpath.2009.11.003.Review.
9. Lam K, Zhang DE. RUNX1 and RUNX1-ETO: roles in hematopoiesis andleukemogenesis. Front Biosci (Landmark Ed). 2012 Jan 1;17:1120-39. Review.
10. Maas S, Shaw A, Bikker H, Hennekam RCM. Trichorhinophalangeal Syndrome. 2017Apr 20. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K,Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University ofWashington, Seattle; 1993-2020. Available fromhttp://www.ncbi.nlm.nih.gov/books/NBK425926/
11. Merchant S, Schlette E, Sanger W, Lai R, Medeiros LJ. Mature B-cell leukemias with more than 55% prolymphocytes: report of 2 cases with Burkitt lymphoma-typechromosomal translocations involving c-myc. Arch Pathol Lab Med. 2003Mar;127(3):305-9. Review.
12. Nusbaum C, Mikkelsen TS, Zody MC, Asakawa S, Taudien S, Garber M, Kodira CD,Schueler MG, Shimizu A, Whittaker CA, Chang JL, Cuomo CA, Dewar K, FitzGerald MG,Yang X, Allen NR, Anderson S, Asakawa T, Blechschmidt K, Bloom T, Borowsky ML,Butler J, Cook A, Corum B, DeArellano K, DeCaprio D, Dooley KT, Dorris L 3rd,Engels R, Glöckner G, Hafez N, Hagopian DS, Hall JL, Ishikawa SK, Jaffe DB, KamatA, Kudoh J, Lehmann R, Lokitsang T, Macdonald P, Major JE, Matthews CD, MauceliE, Menzel U, Mihalev AH, Minoshima S, Murayama Y, Naylor JW, Nicol R, Nguyen C,O'Leary SB, O'Neill K, Parker SC, Polley A, Raymond CK, Reichwald K, Rodriguez J,Sasaki T, Schilhabel M, Siddiqui R, Smith CL, Sneddon TP, Talamas JA, Tenzin P,Topham K, Venkataraman V, Wen G, Yamazaki S, Young SK, Zeng Q, Zimmer AR,Rosenthal A, Birren BW, Platzer M, Shimizu N, Lander ES. DNA sequence andanalysis of human chromosome 8. Nature. 2006 Jan 19;439(7074):331-5.
13. Pienkowska-Grela B, Witkowska A, Grygalewicz B, Rymkiewicz G, Rygier J,Woroniecka R, Walewski J. Frequent aberrations of chromosome 8 in aggressiveB-cell non-Hodgkin lymphoma. Cancer Genet Cytogenet. 2005 Jan 15;156(2):114-21.
14. Smith AC, Spuhler K, Williams TM, McConnell T, Sujansky E, Robinson A. Geneticrisk for recombinant 8 syndrome and the transmission rate of balanced inversion 8in the Hispanic population of the southwestern United States. Am J Hum Genet.1987 Dec;41(6):1083-103.
15. Voigt R, Gburek-Augustat J, Seidel A, Gillessen-Kaesbach G. Hemihyperplasiaand discordant bone age in a patient with trisomy 8 mosaicism. Am J Med Genet A. 2008 Jan 1;146A(1):132-5.
16. Xiao S, Nalabolu SR, Aster JC, Ma J, Abruzzo L, Jaffe ES, Stone R, WeissmanSM, Hudson TJ, Fletcher JA. FGFR1 is fused with a novel zinc-finger gene, ZNF198,in the t(8;13) leukaemia/lymphoma syndrome. Nat Genet. 1998 Jan;18(1):84-7.