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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1987 1
1988 3
1989 4
1990 1
1991 3
1992 5
1993 5
1994 3
1995 3
1996 5
1998 1
1999 2
2000 1
2001 2
2002 2
2003 1
2006 1
2024 0

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43 results

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Page 1
FRAXE and mental retardation.
Mulley JC, Yu S, Loesch DZ, Hay DA, Donnelly A, Gedeon AK, Carbonell P, López I, Glover G, Gabarrón I, et al. Mulley JC, et al. Among authors: gedeon ak. J Med Genet. 1995 Mar;32(3):162-9. doi: 10.1136/jmg.32.3.162. J Med Genet. 1995. PMID: 7783162 Free PMC article.
Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome.
Lower KM, Turner G, Kerr BA, Mathews KD, Shaw MA, Gedeon AK, Schelley S, Hoyme HE, White SM, Delatycki MB, Lampe AK, Clayton-Smith J, Stewart H, van Ravenswaay CM, de Vries BB, Cox B, Grompe M, Ross S, Thomas P, Mulley JC, Gécz J. Lower KM, et al. Among authors: gedeon ak. Nat Genet. 2002 Dec;32(4):661-5. doi: 10.1038/ng1040. Epub 2002 Nov 4. Nat Genet. 2002. PMID: 12415272
Mapping the short arm of human chromosome 16.
Callen DF, Hyland VJ, Baker EG, Fratini A, Gedeon AK, Mulley JC, Fernandez KE, Breuning MH, Sutherland GR. Callen DF, et al. Among authors: gedeon ak. Genomics. 1989 Apr;4(3):348-54. doi: 10.1016/0888-7543(89)90341-8. Genomics. 1989. PMID: 2714795
Mutations in GDI1 are responsible for X-linked non-specific mental retardation.
D'Adamo P, Menegon A, Lo Nigro C, Grasso M, Gulisano M, Tamanini F, Bienvenu T, Gedeon AK, Oostra B, Wu SK, Tandon A, Valtorta F, Balch WE, Chelly J, Toniolo D. D'Adamo P, et al. Among authors: gedeon ak. Nat Genet. 1998 Jun;19(2):134-9. doi: 10.1038/487. Nat Genet. 1998. PMID: 9620768
Experience with direct molecular diagnosis of fragile X.
Mulley JC, Yu S, Gedeon AK, Donnelly A, Turner G, Loesch D, Chapman CJ, Gardner RJ, Richards RI, Sutherland GR. Mulley JC, et al. Among authors: gedeon ak. J Med Genet. 1992 Jun;29(6):368-74. doi: 10.1136/jmg.29.6.368. J Med Genet. 1992. PMID: 1619631 Free PMC article.
The molecular basis of X-linked spondyloepiphyseal dysplasia tarda.
Gedeon AK, Tiller GE, Le Merrer M, Heuertz S, Tranebjaerg L, Chitayat D, Robertson S, Glass IA, Savarirayan R, Cole WG, Rimoin DL, Kousseff BG, Ohashi H, Zabel B, Munnich A, Gecz J, Mulley JC. Gedeon AK, et al. Am J Hum Genet. 2001 Jun;68(6):1386-97. doi: 10.1086/320592. Epub 2001 May 8. Am J Hum Genet. 2001. PMID: 11349230 Free PMC article.
Direct molecular diagnosis of myotonic dystrophy.
Hecht BK, Donnelly A, Gedeon AK, Byard RW, Haan EA, Mulley JC. Hecht BK, et al. Among authors: gedeon ak. Clin Genet. 1993 Jun;43(6):276-85. doi: 10.1111/j.1399-0004.1993.tb03819.x. Clin Genet. 1993. PMID: 8370146
43 results