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Tang, P. Chromosome 13. Encyclopedia. Available online: https://encyclopedia.pub/entry/4677 (accessed on 27 September 2026).
Tang P. Chromosome 13. Encyclopedia. Available at: https://encyclopedia.pub/entry/4677. Accessed September 27, 2026.
Tang, Peter. "Chromosome 13" Encyclopedia, https://encyclopedia.pub/entry/4677 (accessed September 27, 2026).
Tang, P. (2020, December 24). Chromosome 13. In Encyclopedia. https://encyclopedia.pub/entry/4677
Tang, Peter. "Chromosome 13." Encyclopedia. Web. 24 December, 2020.
Chromosome 13
Edit

Humans normally have 46 chromosomes in each cell, divided into 23 pairs. Two copies of chromosome 13, one copy inherited from each parent, form one of the pairs.

chromosomes & mtDNA

References

  1. Baud O, Cormier-Daire V, Lyonnet S, Desjardins L, Turleau C, Doz F. Dysmorphicphenotype and neurological impairment in 22 retinoblastoma patients withconstitutional cytogenetic 13q deletion. Clin Genet. 1999 Jun;55(6):478-82.
  2. de Pontual L, Yao E, Callier P, Faivre L, Drouin V, Cariou S, Van Haeringen A,Geneviève D, Goldenberg A, Oufadem M, Manouvrier S, Munnich A, Vidigal JA,Vekemans M, Lyonnet S, Henrion-Caude A, Ventura A, Amiel J. Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans. Nat Genet.2011 Sep 4;43(10):1026-30. doi: 10.1038/ng.915.
  3. Dunham A, Matthews LH, Burton J, Ashurst JL, Howe KL, Ashcroft KJ, Beare DM,Burford DC, Hunt SE, Griffiths-Jones S, Jones MC, Keenan SJ, Oliver K, Scott CE, Ainscough R, Almeida JP, Ambrose KD, Andrews DT, Ashwell RI, Babbage AK, BagguleyCL, Bailey J, Bannerjee R, Barlow KF, Bates K, Beasley H, Bird CP, Bray-Allen S, Brown AJ, Brown JY, Burrill W, Carder C, Carter NP, Chapman JC, Clamp ME, ClarkSY, Clarke G, Clee CM, Clegg SC, Cobley V, Collins JE, Corby N, Coville GJ,Deloukas P, Dhami P, Dunham I, Dunn M, Earthrowl ME, Ellington AG, Faulkner L,Frankish AG, Frankland J, French L, Garner P, Garnett J, Gilbert JG, Gilson CJ,Ghori J, Grafham DV, Gribble SM, Griffiths C, Hall RE, Hammond S, Harley JL, HartEA, Heath PD, Howden PJ, Huckle EJ, Hunt PJ, Hunt AR, Johnson C, Johnson D, KayM, Kimberley AM, King A, Laird GK, Langford CJ, Lawlor S, Leongamornlert DA,Lloyd DM, Lloyd C, Loveland JE, Lovell J, Martin S, Mashreghi-Mohammadi M,McLaren SJ, McMurray A, Milne S, Moore MJ, Nickerson T, Palmer SA, Pearce AV,Peck AI, Pelan S, Phillimore B, Porter KM, Rice CM, Searle S, Sehra HK, ShownkeenR, Skuce CD, Smith M, Steward CA, Sycamore N, Tester J, Thomas DW, Tracey A,Tromans A, Tubby B, Wall M, Wallis JM, West AP, Whitehead SL, Willey DL, Wilming L, Wray PW, Wright MW, Young L, Coulson A, Durbin R, Hubbard T, Sulston JE, Beck S, Bentley DR, Rogers J, Ross MT. The DNA sequence and analysis of humanchromosome 13. Nature. 2004 Apr 1;428(6982):522-8.
  4. Ensembl Human Map View: Chromosome 13
  5. Gilbert F. Chromosome 13. Genet Test. 2000;4(1):85-94.
  6. Hall HE, Chan ER, Collins A, Judis L, Shirley S, Surti U, Hoffner L, Cockwell AE, Jacobs PA, Hassold TJ. The origin of trisomy 13. Am J Med Genet A. 2007 Oct1;143A(19):2242-8.
  7. Hemmat M, Rumple MJ, Mahon LW, Strom CM, Anguiano A, Talai M, Nguyen B, Boyar FZ. Short stature, digit anomalies and dysmorphic facial features are associated with the duplication of miR-17 ~ 92 cluster. Mol Cytogenet. 2014 Apr 16;7:27.doi: 10.1186/1755-8166-7-27.
  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. Kannu P, Campos-Xavier AB, Hull D, Martinet D, Ballhausen D, Bonafé L.Post-axial polydactyly type A2, overgrowth and autistic traits associated with a chromosome 13q31.3 microduplication encompassing miR-17-92 and GPC5. Eur J MedGenet. 2013 Aug;56(8):452-7. doi: 10.1016/j.ejmg.2013.06.001.Review. Erratum in: Eur J Med Genet. 2014 Feb;57(2-3):123-4.
  10. Kivelä T, Tuppurainen K, Riikonen P, Vapalahti M. Retinoblastoma associatedwith chromosomal 13q14 deletion mosaicism. Ophthalmology. 2003Oct;110(10):1983-8. Review.
  11. UCSC Genome Browser: Statistics
  12. 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.
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