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* [[Síndrome do ollo de gato]]
* [[Methemoglobinemia]]
* [[Esquizofrenia]] <ref name="pmid12477929">{{citeCita journalpublicación periódica |author=Liu H, Abecasis GR, Heath SC, Knowles A, Demars S, Chen YJ, Roos JL, Rapoport JL, Gogos JA, Karayiorgou M |title=Genetic variation in the 22q11 locus and susceptibility to schizophrenia |journal=[[Proc. Natl. Acad. Sci. U.S.A.]] |volume=99 |issue=26 |pages=16859–64 |year=2002 |month=December |pmid=12477929 |pmc=139234 |doi=10.1073/pnas.232186099 |url=http://www.pnas.org/cgi/pmidlookup?view=long&pmid=12477929}}</ref>
== Trastornos cromosómicos ==
== Notas ==
{{listaref}}
* {{citeCita journalpublicación periódica | author=Dunham I, Shimizu N, Roe BA, Chissoe S, Hunt AR, Collins JE, Bruskiewich R, Beare DM, Clamp M, Smink LJ, Ainscough R, Almeida JP, Babbage A, Bagguley C, Bailey J, Barlow K, Bates KN, Beasley O, Bird CP, Blakey S, Bridgeman AM, Buck D, Burgess J, Burrill WD, O'Brien KP | title=The DNA sequence of human chromosome 22 | journal=Nature | year=1999 | pages=489–95 | volume=402 | issue=6761 | pmid=10591208 | doi=10.1038/990031}}
* {{citeCita journalpublicación periódica | author=Gilbert F | title=Disease genes and chromosomes: disease maps of the human genome. Chromosome 22 | journal=Genet Test | year=1998 | pages=89–97 | volume=2 | issue=1 | pmid=10464604 | doi=10.1089/gte.1998.2.89}}
* {{citeCita journalpublicación periódica | author=Kurzrock R, Kantarjian HM, Druker BJ, Talpaz M | title=Philadelphia chromosome-positive leukemias: from basic mechanisms to molecular therapeutics | journal=Ann Intern Med | year=2003 | pages=819–30 | volume=138 | issue=10 | pmid=12755554}}
* {{citeCita journalpublicación periódica | author=Maynard TM, Haskell GT, Lieberman JA, LaMantia AS | title=22q11 DS: genomic mechanisms and gene function in DiGeorge/velocardiofacial syndrome | journal=Int J Dev Neurosci | year=2002 | pages=407–19 | volume=20 | issue=3–5 | pmid=12175881 | doi=10.1016/S0736-5748(02)00050-3}}
* {{citeCita journalpublicación periódica | author=McDermid HE, Morrow BE | title=Genomic disorders on 22q11 | journal=Am J Hum Genet | year=2002 | pages=1077–88 | volume=70 | issue=5 | pmid=11925570 | doi=10.1086/340363 | pmc=447586}}
* {{citeCita journalpublicación periódica | author=McDonald-McGinn DM, Kirschner R, Goldmuntz E, Sullivan K, Eicher P, Gerdes M, Moss E, Solot C, Wang P, Jacobs I, Handler S, Knightly C, Heher K, Wilson M, Ming JE, Grace K, Driscoll D, Pasquariello P, Randall P, Larossa D, Emanuel BS, Zackai EH | title=The Philadelphia story: the 22q11.2 deletion: report on 250 patients | journal=Genet Couns | year=1999 | pages=11–24 | volume=10 | issue=1 | pmid=10191425}}
* {{citeCita journalpublicación periódica | author=Rinn JL, Euskirchen G, Bertone P, Martone R, Luscombe NM, Hartman S, Harrison PM, Nelson FK, Miller P, Gerstein M, Weissman S, Snyder M | title=The transcriptional activity of human Chromosome 22 | journal=Genes Dev | year=2003 | pages=529–40 | volume=17 | issue=4 | pmid=12600945 | doi=10.1101/gad.1055203 | pmc=195998}}
* {{citeCita journalpublicación periódica | author = Wilson HL, Wong ACC, Shaw SR, Tse WY, Stapleton GA, Phelan MC, Hu S, Marshall J, McDermid HE ''et al.'' | year = 2003 | title = Molecular characerisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSASP2 in the major neurological symptoms | url = | journal = J Med Genet | volume = 40 | issue = | pages = 575–584 | doi = 10.1136/jmg.40.8.575 | pmid = 12920066 | pmc=1735560}}
{{Cromosomas humanos}}
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