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Chromosom 20 - Wikipedia, wolna encyklopedia

Chromosom 20

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Chromosom 20 – jeden z 23 parzystych chromosomów człowieka. DNA chromosomu 20 liczy około 63 milionów par nukleotydów, co stanowi od 2 do 2,5% materiału genetycznego ludzkiej komórki[1]. Chromosom 20 jest jednym z najmniejszych ludzkich chromosomów. Liczbę genów chromosomu 20 szacuje się na około 900.

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[edytuj] Bibliografia

  • Deloukas, P, Matthews, LH, Ashurst, J, Burton, J, Gilbert, JG, Jones, M, Stavrides, G, Almeida, JP, Babbage, AK, Bagguley, CL, Bailey, J, Barlow, KF, Bates, KN, Beard, LM, Beare, DM, Beasley, OP, Bird, CP, Blakey, SE, Bridgeman, AM, Brown, AJ, Buck, D, Burrill, W, Butler, AP, Carder, C, Carter, NP, Chapman, JC, Clamp, M, Clark, G, Clark, LN, Clark, SY, Clee, CM, Clegg, S, Cobley, VE, Collier, RE, Connor, R, Corby, NR, Coulson, A, Coville, GJ, Deadman, R, Dhami, P, Dunn, M, Ellington, AG, Frankland, JA, Fraser, A, French, L, Garner, P, Grafham, DV, Griffiths, C, Griffiths, MN, Gwilliam, R, Hall, RE, Hammond, S, Harley, JL, Heath, PD, Ho, S, Holden, JL, Howden, PJ, Huckle, E, Hunt, AR, Hunt, SE, Jekosch, K, Johnson, CM, Johnson, D, Kay, MP, Kimberley, AM, King, A, Knights, A, Laird, GK, Lawlor, S, Lehvaslaiho, MH, Leversha, M, Lloyd, C, Lloyd, DM, Lovell, JD, Marsh, VL, Martin, SL, McConnachie, LJ, McLay, K, McMurray, AA, Milne, S, Mistry, D, Moore, MJ, Mullikin, JC, Nickerson, T, Oliver, K, Parker, A, Patel, R, Pearce, TA, Peck, AI, Phillimore, BJ, Prathalingam, SR, Plumb, RW, Ramsay, H, Rice, CM, Ross, MT, Scott, CE, Sehra, HK, Shownkeen, R, Sims, S, Skuce, CD, Smith, ML, Soderlund, C, Steward, CA, Sulston, JE, Swann, M, Sycamore, N, Taylor, R, Tee, L, Thomas, DW, Thorpe, A, Tracey, A, Tromans, AC, Vaudin, M, Wall, M, Wallis, JM, Whitehead, SL, Whittaker, P, Willey, DL, Williams, L, Williams, SA, Wilming, L, Wray, PW, Hubbard, T, Durbin, RM, Bentley, DR, Beck, S, Rogers, J. The DNA sequence and comparative analysis of human chromosome 20. Nature. 414, 6866, 865-871. 2001. PMID 11780052.
  • Gilbert, F. Disease genes and chromosomes: disease maps of the human genome. Genetic Testing. 1, 3, 225-229. 1997. PMID 10464650.

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