Donnelly A - Search Results

1

A linkage map of microsatellite markers on the human X chromosome.

Donnelly A, Kozman H, Gedeon AK, Webb S, Lynch M, Sutherland GR, Richards RI, Mulley JC. Donnelly A, et al. Genomics. 1994 Apr;20(3):363-70. doi: 10.1006/geno.1994.1189. Genomics. 1994. PMID: 8034308

2

Regional localisation of a non-specific X-linked mental retardation gene (MRX19) to Xp22.

Donnelly AJ, Choo KH, Kozman HM, Gedeon AK, Danks DM, Mulley JC. Donnelly AJ, et al. Am J Med Genet. 1994 Jul 15;51(4):581-5. doi: 10.1002/ajmg.1320510457. Am J Med Genet. 1994. PMID: 7943043

3

Localisation of the gene for X-linked reticulate pigmentary disorder with systemic manifestations (PDR), previously known as X-linked cutaneous amyloidosis.

Gedeon AK, Mulley JC, Kozman H, Donnelly A, Partington MW. Gedeon AK, et al. Among authors: donnelly a. Am J Med Genet. 1994 Aug 1;52(1):75-8. doi: 10.1002/ajmg.1320520115. Am J Med Genet. 1994. PMID: 7977467

4

Characterization of the human glutamate receptor subunit 3 gene (GRIA3), a candidate for bipolar disorder and nonspecific X-linked mental retardation.

Gécz J, Barnett S, Liu J, Hollway G, Donnelly A, Eyre H, Eshkevari HS, Baltazar R, Grunn A, Nagaraja R, Gilliam C, Peltonen L, Sutherland GR, Baron M, Mulley JC. Gécz J, et al. Among authors: donnelly a. Genomics. 1999 Dec 15;62(3):356-68. doi: 10.1006/geno.1999.6032. Genomics. 1999. PMID: 10644433

5

Regional localisation of two non-specific X-linked mental retardation genes (MRX30 and MRX31).

Donnelly AJ, Partington MW, Ryan AK, Mulley JC. Donnelly AJ, et al. Am J Med Genet. 1996 Jul 12;64(1):113-20. doi: 10.1002/(SICI)1096-8628(19960712)64:1<113::AID-AJMG19>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 8826460

6

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: donnelly a. Am J Hum Genet. 1992 May;50(5):968-80. Am J Hum Genet. 1992. PMID: 1570846 Free PMC article.

7

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: donnelly a. 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.

8

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: donnelly 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.

9

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: donnelly a. 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.

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: donnelly a. 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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