Citations for

1	DIS3, DIS3L, DIS3L2, PRLMNS
	Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility.
	Astuti D, Morris MR, Cooper WN, Staals RH, Wake NC, Fews GA, Gill H, Gentle D, Shuib S, Ricketts CJ, Cole T, van Essen AJ, van Lingen RA, Neri G, Opitz JM, Rump P, Stolte-Dijkstra I, Müller F, Pruijn GJ, Latif F, Maher ER.
	Nat Genet 44(3):277-84. doi: 10.1038/ng.1071. 2012
2	DIS3, DIS3L
	Dis3-like 1: a novel exoribonuclease associated with the human exosome.
	Staals RH, Bronkhorst AW, Schilders G, Slomovic S, Schuster G, Heck AJ, Raijmakers R, Pruijn GJ.
	EMBO J 29(14):2358-67. doi: 10.1038/emboj.2010.122. Epub 2010 Jun 8. 2010
3	DIS3, DIS3L
	The human core exosome interacts with differentially localized processive RNases: hDIS3 and hDIS3L.
	Tomecki R, Kristiansen MS, Lykke-Andersen S, Chlebowski A, Larsen KM, Szczesny RJ, Drazkowska K, Pastula A, Andersen JS, Stepien PP, Dziembowski A, Jensen TH.
	EMBO J 29(14):2342-57. doi: 10.1038/emboj.2010.121. Epub 2010 Jun 8. 2010
4	AARSD1, ACSM2A, ACTL8, ADAD2, ADAM6, AGAP9, AHCTF1P, ALDH1L2, AMER1, AMN1, ANGEL2, ANKFN1, ANKHD1, ANKIB1, ANKMY2, ANKRD10, ANKRD18A, ANKRD19, ANKRD26, ANKRD27, ANKRD31, ANKRD33, ANKRD34A, ANKRD34C, ANKRD35, ANKRD50, ANKS6, ARMC5, ATAD2B, ATP5SL, ATP5Sl, BTBD11, C10orf139, C10orf31, C11orf37, C11orf39, C11orf44, C11orf55, C12orf27, C12orf35, C12orf40, C12orf47, C12orf50, C12orf55, C14orf105, C14orf180, C14orf181, C14orf70, C15orf28, C15orf37, C15orf53, C15orf54, C15orf56, C16orf13, C16orf59, C16orf68, C16orf81, C17orf47, C17orf53, C17orf55, C17orf56, C17orf65, C17orf66, C17orf69, C17orf72, C17orf76, C17orf77, C17orf78, C18orf15, C18orf26, C18orf33, C18orf62, C19orf46, C1orf112, C1orf125, C1orf127, C1orf131, C1orf132, C1orf62, C1orf83, C1orf92, C1orf96, C20orf152, C20orf175, C20orf200, C20orf46, C21orf125, C21orf130, C22orf37, C2orf54, C2orf61, C2orf67, C3orf30, C3orf41, C3orf44, C3orf56, C4orf21, C4orf30, C4orf32, C4orf35, C5orf17, C5orf30, C5orf34, C6orf103, C6orf140, C6orf147, C6orf214, C7orf40, C7orf42, C7orf52, C8orf31, C8orf34, C8orf47, C9orf106, C9orf139, C9orf66, C9orf73, C9orf97, CALML4, CBR4, CC2D2A, CCDC114, CCDC115, CCDC121, CCDC128, CCDC129, CCDC138, CCDC140, CCDC141, CCDC144B, CCDC148, CCDC43, CCDC57, CCDC63, CCDC65, CCDC69, CCDC83, CCDC87, CCDC93, CCDC97, CCNJ, CCNJL, CCT6AP1, CDC20B, CEP164, CEP170B, CKAP2L, CLEC4GP1, CNTD2, CNTNAP5, COA1, CROCCL1, CROCCL2, CXorf18, CXorf25, CXorf55, CXorf62, CYP4V2, DCAF17, DDX60, DEF8, DEPDC1B, DEPDC4, DHRS12, DIS3L, DNAAF3, DNHD1, DNHD1L, DNHL1, DTWD2, DUSP27, DZIP1L, ECHDC2, EHBP1L1, EOGT, EP400NL, FADS6, FAM108C1, FAM133A, FAM134A, FAM139A, FAM149A, FAM149B1, FAM153C, FAM173B, FAM182A, FAM21A, FAM21C, FAM45A, FAM66A, FAM66B, FAM66C, FAM66D, FAM66E, FAM71D, FAM73A, FAM75C1, FAM78A, FAM87B, FAM90A1, FAM98A, FAM98B, FAM98C, FLAD1, FSD2, GAB4, GARIN1B, GARNL3, GAS2L3, GK5, GLYATL1, GMPPA, GOLGA9P, GSTCD, H2BFM, HDX, HECTD2, HFM1, IFTAP, IGSF22, IGSF5, ISLR2, KANK2, KANK3, KANK4, KCTD19, KIAA0913, KIAA1324L, KIF24, KLHDC7A, KLHL26, L3MBTL4, LARP6, LBA1, LIME1, LINC00299, LOXHD1, LRRC36, LRRC37A4, MARCH9, MIB2, MOBKL1B, MOBKL2A, MOBKL2B, MOBKL2C, MORC4, MTURN, MYH15, N6AMT1, NAA30, NAG8, NDUFAF5, NKAIN3, NOXIN, NUBPL, OTOGL, OTOGL, PDZK1P1, PHF20L1, PIANP, PID1, PLCH1, POLR3D, PROX2, PRR10, RANBP6, RETREG3, RFPL4B, RIPPLY2, RITA1, SCIMP, SDE2, SETD4, SFXN4, SIRPD, SLC10A5, SLC25A29, SLC35E1, SLC35F1, SLC35F3, SLC38A10, SLC38A11, SLC38A7, SMAGP, SMG8, SMYD4, SNHG10, SNHG11, SNX30, STAG3L1, SWSAP1, TANC2, TBRG4, TDRD7, TERB1, TMEM105, TMEM151B, TMEM222, TPD52L3, TRMT2B, TSGA10IP, TTC29, UAP1L1, VPS35L, WDR63, WDR90, WDTC1, ZBTB46, ZIK1, ZMAT1, ZMAT2, ZNF12, ZNF321, ZNF347, ZNF430, ZNF433, ZNF441, ZNF442, ZNF483, ZNF526, ZNF527, ZNF569, ZNF600, ZNF615, ZNF619, ZNF620, ZNF662, ZNFX1, ZYG11B, ZZZ3
	Complete sequencing and characterization of 21,243 full-length human cDNAs.
	Ota T, Suzuki Y, Nishikawa T, Otsuki T, Sugiyama T, Irie R, Wakamatsu A, Hayashi K, Sato H, Nagai K, Kimura K, Makita H, Sekine M, Obayashi M, Nishi T, Shibahara T, Tanaka T, Ishii S, Yamamoto J, Saito K, Kawai Y, Isono Y, Nakamura Y, Nagahari K, Murakami K, Yasuda T, Iwayanagi T, Wagatsuma M, Shiratori A, Sudo H, Hosoiri T, Kaku Y, Kodaira H, Kondo H, Sugawara M, Takahashi M, Kanda K, Yokoi T, Furuya T, Kikkawa E, Omura Y, Abe K, Kamihara K, Katsuta N, Sato K, Tanikawa M, Yamazaki M, Ninomiya K, Ishibashi T, Yamashita H, Murakawa K, Fujimori K, Tanai H, Kimata M, Watanabe M, Hiraoka S, Chiba Y, Ishida S, Ono Y, Takiguchi S, Watanabe S, Yosida M, Hotuta T, Kusano J, Kanehori K, Takahashi-Fujii A, Hara H, Tanase TO, Nomura Y, Togiya S, Komai F, Hara R, Takeuchi K, Arita M, Imose N, Musashino K, Yuuki H, Oshima A, Sasaki N, Aotsuka S, Yoshikawa Y, Matsunawa H, Ichihara T, Shiohata N, Sano S, Moriya S, Momiyama H, Satoh N, Takami S, Terashima Y, Suzuki O, Nakagawa S, Senoh A, Mizoguchi H, Goto Y, Shimizu F, Wakebe H, Hishigaki H, Watanabe T, Sugiyama A, Takemoto M, Kawakami B, Yamazaki M, Watanabe K, Kumagai A, Itakura S, Fukuzumi Y, Fujimori Y, Komiyama M, Tashiro H, Tanigami A, Fujiwara T, Ono T, Yamada K, Fujii Y, Ozaki K, Hirao M, Ohmori Y, Kawabata A, Hikiji T, Kobatake N, Inagaki H, Ikema Y, Okamoto S, Okitani R, Kawakami T, Noguchi S, Itoh T, Shigeta K, Senba T, Matsumura K, Nakajima Y, Mizuno T, Morinaga M, Sasaki M, Togashi T, Oyama M, Hata H, Watanabe M, Komatsu T, Mizushima-Sugano J, Satoh T, Shirai Y, Takahashi Y, Nakagawa K, Okumura K, Nagase T, Nomura N, Kikuchi H, Masuho Y, Yamashita R, Nakai K, Yada T, Nakamura Y, Ohara O, Isogai T, Sugano S.
	Nat Genet 36(1):40-5. Epub 2003 Dec 21. 2004