Citations for

1	FGD1, FGD2, FGD3, FGD4
	Frabin and other related Cdc42-specific guanine nucleotide exchange factors couple the actin cytoskeleton with the plasma membrane.
	Nakanishi H, Takai Y.
	J Cell Mol Med 12(4):1169-76. Epub 2008 Apr 9. Review. 2008
2	FGD1, FGD3
	Novel insights into FGD3, a putative GEF for Cdc42, that undergoes SCF(FWD1/beta-TrCP)-mediated proteasomal degradation analogous to that of its homologue FGD1 but regulates cell morphology and motility differently from FGD1.
	Hayakawa M, Matsushima M, Hagiwara H, Oshima T, Fujino T, Ando K, Kikugawa K, Tanaka H, Miyazawa K, Kitagawa M.
	Genes Cells 13(4):329-42. 2008
3	FGD1, FGD2, FGD3, FGD4
	FGD2, a CDC42-specific exchange factor expressed by antigen-presenting cells, localizes to early endosomes and active membrane ruffles.
	Huber C, Mårtensson A, Bokoch GM, Nemazee D, Gavin AL.
	J Biol Chem 283(49):34002-12. Epub 2008 Oct 6. 2008
4	ACTL7A, ACTL7B, ANKRD18B, ANKRD20A2, ANKRD20A3, ANKRD20A4, ARRDC1, C9orf114, C9orf118, C9orf122, C9orf123, C9orf125, C9orf130, C9orf134, C9orf135, C9orf142, C9orf29, C9orf71, C9orf72, CBWD6, CBWD7, CNTLN, DCTN3, DMRT3, FAM189A2, FAM27D1, FAM27E1, FAM27E2, FAM74A1, FAM74A3, FAM74A4, FAM75A1, FGD3, FOXB2, FOXD4, FOXD4L5, GLT6D1, IARS, KIAA1045, KIAA2026, MED27, MEGF9, MOST2, PALM2, RABEPK, RFX3, SCAI, SMU1, ZCCHC7, ZDHHC12
	DNA sequence and analysis of human chromosome 9.
	Humphray SJ, Oliver K, Hunt AR, Plumb RW, Loveland JE, Howe KL, Andrews TD, Searle S, Hunt SE, Scott CE, Jones MC, Ainscough R, Almeida JP, Ambrose KD, Ashwell RI, Babbage AK, Babbage S, Bagguley CL, Bailey J, Banerjee R, Barker DJ, Barlow KF, Bates K, Beasley H, Beasley O, Bird CP, Bray-Allen S, Brown AJ, Brown JY, Burford D, Burrill W, Burton J, Carder C, Carter NP, Chapman JC, Chen Y, Clarke G, Clark SY, Clee CM, Clegg S, Collier RE, Corby N, Crosier M, Cummings AT, Davies J, Dhami P, Dunn M, Dutta I, Dyer LW, Earthrowl ME, Faulkner L, Fleming CJ, Frankish A, Frankland JA, French L, Fricker DG, Garner P, Garnett J, Ghori J, Gilbert JG, Glison C, Grafham DV, Gribble S, Griffiths C, Griffiths-Jones S, Grocock R, Guy J, Hall RE, Hammond S, Harley JL, Harrison ES, Hart EA, Heath PD, Henderson CD, Hopkins BL, Howard PJ, Howden PJ, Huckle E, Johnson C, Johnson D, Joy AA, Kay M, Keenan S, Kershaw JK, Kimberley AM, King A, Knights A, Laird GK, Langford C, Lawlor S, Leongamornlert DA, Leversha M, Lloyd C, Lloyd DM, Lovell J, Martin S, Mashreghi-Mohammadi M, Matthews L, McLaren S, McLay KE, McMurray A, Milne S, Nickerson T, Nisbett J, Nordsiek G, Pearce AV, Peck AI, Porter KM, Pandian R, Pelan S, Phillimore B, Povey S, Ramsey Y, Rand V, Scharfe M, Sehra HK, Shownkeen R, Sims SK, Skuce CD, Smith M, Steward CA, Swarbreck D, Sycamore N, Tester J, Thorpe A, Tracey A, Tromans A, Thomas DW, Wall M, Wallis JM, West AP, Whitehead SL, Willey DL, Williams SA, Wilming L, Wray PW, Young L, Ashurst JL, Coulson A, Bl�cker H, Durbin R, Sulston JE, Hubbard T, Jackson MJ, Bentley DR, Beck S, Rogers J, Dunham I.
	Nature 429(6990):369-74. 2004
5	ECM2, FGD3, HSAN1, NINJ1, OGN, OMD, ROR2, SPTLC1
	SPTLC1 is mutated in hereditary sensory neuropathy, type 1.
	Bejaoui K, Wu C, Scheffler MD, Haan G, Ashby P, Wu L, de Jong P, Brown RH Jr.
	Nat Genet 27(3):261-2. 2001
6	FGD1, FGD3
	Isolation, characterization, and mapping of the mouse Fgd3 gene, a new Faciogenital Dysplasia (FGD1; Aarskog Syndrome) gene homologue.
	Pasteris NG, Nagata K, Hall A, Gorski JL.
	Gene 242(1-2):237-47. 2000