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Line 294: * {{cite journal \|vauthors=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}} * {{cite journal \|vauthors=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}} * {{cite journal \|vauthors=Wilson HL, Wong AC, Shaw SR, Tse WY, Stapleton GA, Phelan MC, Hu S, Marshall J, McDermid HE \| year = 2003 \| title = Molecular characterisation 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 = 8\| pages = 575–584 \| doi = 10.1136/jmg.40.8.575 \| pmid = 12920066 \| pmc=1735560\|display-authors=etal}} ==External links==

Chromosome 22: Difference between revisions