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Tang, P. Chromosome 12. Encyclopedia. Available online: https://encyclopedia.pub/entry/4672 (accessed on 25 September 2026).
Tang P. Chromosome 12. Encyclopedia. Available at: https://encyclopedia.pub/entry/4672. Accessed September 25, 2026.
Tang, Peter. "Chromosome 12" Encyclopedia, https://encyclopedia.pub/entry/4672 (accessed September 25, 2026).
Tang, P. (2020, December 24). Chromosome 12. In Encyclopedia. https://encyclopedia.pub/entry/4672
Tang, Peter. "Chromosome 12." Encyclopedia. Web. 24 December, 2020.
Chromosome 12
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Humans normally have 46 chromosomes in each cell, divided into 23 pairs. Two copies of chromosome 12, one copy inherited from each parent, form one of the pairs.

chromosomes & mtDNA

References

  1. Dim DC, Cooley LD, Miranda RN. Clear cell sarcoma of tendons and aponeuroses: a review. Arch Pathol Lab Med. 2007 Jan;131(1):152-6. Review.
  2. Dufke A, Walczak C, Liehr T, Starke H, Trifonov V, Rubtsov N, Schöning M,Enders H, Eggermann T. Partial tetrasomy 12pter-12p12.3 in a girl withPallister-Killian syndrome: extraordinary finding of an analphoid, invertedduplicated marker. Eur J Hum Genet. 2001 Aug;9(8):572-6.
  3. Ensembl Human Map View: Chromosome 12
  4. Gilbert F, Kauff N. Disease genes and chromosomes: disease maps of the humangenome.Chromosome 12. Genet Test. 2000;4(3):319-33.
  5. Haferlach C, Bacher U, Schnittger S, Alpermann T, Zenger M, Kern W, Haferlach T. ETV6 rearrangements are recurrent in myeloid malignancies and are frequentlyassociated with other genetic events. Genes Chromosomes Cancer. 2012Apr;51(4):328-37. doi: 10.1002/gcc.21918.
  6. Italiano A, Cardot N, Dupré F, Monticelli I, Keslair F, Piche M, Mainguené C, Coindre JM, Pedeutour F. Gains and complex rearrangements of the 12q13-15chromosomal region in ordinary lipomas: the "missing link" between lipomas andliposarcomas? Int J Cancer. 2007 Jul 15;121(2):308-15.
  7. Leube B, Majewski F, Gebauer J, Royer-Pokora B. Clinical, cytogenetic, andmolecular observations in a patient with Pallister-Killian-syndrome with anunusual karyotype. Am J Med Genet A. 2003 Dec 15;123A(3):296-300.
  8. Montgomery KT, Lee E, Miller A, Lau S, Shim C, Decker J, Chiu D, Emerling S,Sekhon M, Kim R, Lenz J, Han J, Ioshikhes I, Renault B, Marondel I, Yoon SJ, SongK, Murty VV, Scherer S, Yonescu R, Kirsch IR, Ried T, McPherson J, Gibbs R,Kucherlapati R. A high-resolution map of human chromosome 12. Nature. 2001 Feb15;409(6822):945-6.
  9. Porpaczy E, Bilban M, Heinze G, Gruber M, Vanura K, Schwarzinger I,Stilgenbauer S, Streubel B, Fonatsch C, Jaeger U. Gene expression signature ofchronic lymphocytic leukaemia with Trisomy 12. Eur J Clin Invest. 2009Jul;39(7):568-75. doi: 10.1111/j.1365-2362.2009.02146.x.
  10. Scherer SE, Muzny DM, Buhay CJ, Chen R, Cree A, Ding Y, Dugan-Rocha S, Gill R,Gunaratne P, Harris RA, Hawes AC, Hernandez J, Hodgson AV, Hume J, Jackson A,Khan ZM, Kovar-Smith C, Lewis LR, Lozado RJ, Metzker ML, Milosavljevic A, MinerGR, Montgomery KT, Morgan MB, Nazareth LV, Scott G, Sodergren E, Song XZ, SteffenD, Lovering RC, Wheeler DA, Worley KC, Yuan Y, Zhang Z, Adams CQ, Ansari-Lari MA,Ayele M, Brown MJ, Chen G, Chen Z, Clerc-Blankenburg KP, Davis C, Delgado O, DinhHH, Draper H, Gonzalez-Garay ML, Havlak P, Jackson LR, Jacob LS, Kelly SH, Li L, Li Z, Liu J, Liu W, Lu J, Maheshwari M, Nguyen BV, Okwuonu GO, Pasternak S, PerezLM, Plopper FJ, Santibanez J, Shen H, Tabor PE, Verduzco D, Waldron L, Wang Q,Williams GA, Zhang J, Zhou J, Allen CC, Amin AG, Anyalebechi V, Bailey M,Barbaria JA, Bimage KE, Bryant NP, Burch PE, Burkett CE, Burrell KL, Calderon E, Cardenas V, Carter K, Casias K, Cavazos I, Cavazos SR, Ceasar H, Chacko J, ChanSN, Chavez D, Christopoulos C, Chu J, Cockrell R, Cox CD, Dang M, Dathorne SR,David R, Davis CM, Davy-Carroll L, Deshazo DR, Donlin JE, D'Souza L, Eaves KA,Egan A, Emery-Cohen AJ, Escotto M, Flagg N, Forbes LD, Gabisi AM, Garza M,Hamilton C, Henderson N, Hernandez O, Hines S, Hogues ME, Huang M, Idlebird DG,Johnson R, Jolivet A, Jones S, Kagan R, King LM, Leal B, Lebow H, Lee S, LeVanJM, Lewis LC, London P, Lorensuhewa LM, Loulseged H, Lovett DA, Lucier A, Lucier RL, Ma J, Madu RC, Mapua P, Martindale AD, Martinez E, Massey E, Mawhiney S,Meador MG, Mendez S, Mercado C, Mercado IC, Merritt CE, Miner ZL, Minja E,Mitchell T, Mohabbat F, Mohabbat K, Montgomery B, Moore N, Morris S, Munidasa M, Ngo RN, Nguyen NB, Nickerson E, Nwaokelemeh OO, Nwokenkwo S, Obregon M, Oguh M,Oragunye N, Oviedo RJ, Parish BJ, Parker DN, Parrish J, Parks KL, Paul HA, PaytonBA, Perez A, Perrin W, Pickens A, Primus EL, Pu LL, Puazo M, Quiles MM, QuirozJB, Rabata D, Reeves K, Ruiz SJ, Shao H, Sisson I, Sonaike T, Sorelle RP, Sutton AE, Svatek AF, Svetz LA, Tamerisa KS, Taylor TR, Teague B, Thomas N, Thorn RD,Trejos ZY, Trevino BK, Ukegbu ON, Urban JB, Vasquez LI, Vera VA, Villasana DM,Wang L, Ward-Moore S, Warren JT, Wei X, White F, Williamson AL, Wleczyk R, WoodenHS, Wooden SH, Yen J, Yoon L, Yoon V, Zorrilla SE, Nelson D, Kucherlapati R,Weinstock G, Gibbs RA; Baylor College of Medicine Human Genome Sequencing Center Sequence Production Team. The finished DNA sequence of human chromosome 12.Nature. 2006 Mar 16;440(7082):346-51.
  11. Struthers JL, Cuthbert CD, Khalifa MM. Parental origin of the isochromosome12p in Pallister-Killian syndrome: molecular analysis of one patient and reviewof the reported cases. Am J Med Genet. 1999 May 21;84(2):111-5. Review.
  12. Thway K. Angiomatoid fibrous histiocytoma: a review with recent geneticfindings. Arch Pathol Lab Med. 2008 Feb;132(2):273-7. doi:10.1043/1543-2165(2008)132[273:AFHARW]2.0.CO;2. Review.
  13. UCSC Genome Browser: Statistics
  14. Yeung A, Francis D, Giouzeppos O, Amor DJ. Pallister-Killian syndrome causedby mosaicism for a supernumerary ring chromosome 12p. Am J Med Genet A. 2009Mar;149A(3):505-9. doi: 10.1002/ajmg.a.32664.
  15. Zhou MH, Gao L, Jing Y, Xu YY, Ding Y, Wang N, Wang W, Li MY, Han XP, Sun JZ, Wang LL, Yu L. Detection of ETV6 gene rearrangements in adult acute lymphoblasticleukemia. Ann Hematol. 2012 Aug;91(8):1235-43. doi: 10.1007/s00277-012-1431-4.
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Update Date: 24 Dec 2020
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