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Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy.
Strømme P, Mangelsdorf ME, Shaw MA, Lower KM, Lewis SM, Bruyere H, Lütcherath V, Gedeon AK, Wallace RH, Scheffer IE, Turner G, Partington M, Frints SG, Fryns JP, Sutherland GR, Mulley JC, Gécz J. Strømme P, et al. Among authors: gedeon ak. Nat Genet. 2002 Apr;30(4):441-5. doi: 10.1038/ng862. Epub 2002 Mar 11. Nat Genet. 2002. PMID: 11889467
Refined genetic localization for central core disease.
Mulley JC, Kozman HM, Phillips HA, Gedeon AK, McCure JA, Iles DE, Gregg RG, Hogan K, Couch FJ, MacLennan DH, et al. Mulley JC, et al. Among authors: gedeon ak. Am J Hum Genet. 1993 Feb;52(2):398-405. Am J Hum Genet. 1993. PMID: 8430700 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
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.
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
61 results