Gedeon A - Search Results

1

Fragile-X syndrome: unique genetics of the heritable unstable element.

Yu S, Mulley J, Loesch D, Turner G, Donnelly A, Gedeon A, Hillen D, Kremer E, Lynch M, Pritchard M, et al. Yu S, et al. Among authors: gedeon a. Am J Hum Genet. 1992 May;50(5):968-80. Am J Hum Genet. 1992. PMID: 1570846 Free PMC article.

2

Localization of non-specific X-linked mental retardation genes.

Kerr B, Gedeon A, Mulley J, Turner G. Kerr B, et al. Among authors: gedeon a. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):392-401. doi: 10.1002/ajmg.1320430160. Am J Med Genet. 1992. PMID: 1605217

3

Prenatal diagnosis of fragile X syndrome by direct detection of the unstable DNA sequence.

Sutherland GR, Gedeon A, Kornman L, Donnelly A, Byard RW, Mulley JC, Kremer E, Lynch M, Pritchard M, Yu S, et al. Sutherland GR, et al. Among authors: gedeon a. N Engl J Med. 1991 Dec 12;325(24):1720-2. doi: 10.1056/NEJM199112123252407. N Engl J Med. 1991. PMID: 1944473 Free article. No abstract available.

4

Pericentromeric genes for non-specific X-linked mental retardation (MRX).

Gedeon A, Kerr B, Mulley J, Turner G. Gedeon A, et al. Am J Med Genet. 1994 Jul 15;51(4):553-64. doi: 10.1002/ajmg.1320510453. Am J Med Genet. 1994. PMID: 7943039

5

X-linked mental retardation with heterozygous expression and macrocephaly: pericentromeric gene localization.

Turner G, Gedeon A, Mulley J. Turner G, et al. Among authors: gedeon a. Am J Med Genet. 1994 Jul 15;51(4):575-80. doi: 10.1002/ajmg.1320510456. Am J Med Genet. 1994. PMID: 7943042

6

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.

7

A linkage group with FRA16B (the fragile site at 16q22.1).

Mulley JC, Hyland VJ, Fratini A, Bates LJ, Gedeon AK, Sutherland GR. Mulley JC, et al. Among authors: gedeon ak. Hum Genet. 1989 May;82(2):131-3. doi: 10.1007/BF00284044. Hum Genet. 1989. PMID: 2722188

8

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.

9

Genotype-phenotype relationships in fragile X syndrome: a family study.

Loesch DZ, Huggins R, Hay DA, Gedeon AK, Mulley JC, Sutherland GR. Loesch DZ, et al. Among authors: gedeon ak. Am J Hum Genet. 1993 Nov;53(5):1064-73. Am J Hum Genet. 1993. PMID: 8213832 Free PMC article.

10

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

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