Dye D - Search Results

1

Using genetic epidemiology to study Rett syndrome: the design of a case-control study.

Leonard H, Fyfe S, Dye D, Leonard S. Leonard H, et al. Among authors: dye d. Paediatr Perinat Epidemiol. 2000 Jan;14(1):85-95. doi: 10.1046/j.1365-3016.2000.00218.x. Paediatr Perinat Epidemiol. 2000. PMID: 10703039

2

Familial aggregation in Rett syndrome: what is the evidence for clustering of other disorders in families of affected girls?

Leonard H, Fyfe S, Dye D, Leonard S. Leonard H, et al. Among authors: dye d. Am J Med Genet. 1999 Jan 29;82(3):228-34. doi: 10.1002/(sici)1096-8628(19990129)82:3<228::aid-ajmg7>3.0.co;2-k. Am J Med Genet. 1999. PMID: 10215546

3

Patterns of pregnancy loss, perinatal mortality, and postneonatal childhood deaths in families of girls with Rett syndrome.

Fyfe S, Leonard H, Dye D, Leonard S. Fyfe S, et al. Among authors: dye d. J Child Neurol. 1999 Jul;14(7):440-5. doi: 10.1177/088307389901400706. J Child Neurol. 1999. PMID: 10573466

4

Family data in Rett syndrome: association with other genetic disorders.

Leonard H, Fyfe S, Dye D, Hockey A, Christodoulou J. Leonard H, et al. Among authors: dye d. J Paediatr Child Health. 2000 Aug;36(4):336-9. doi: 10.1046/j.1440-1754.2000.00531.x. J Paediatr Child Health. 2000. PMID: 10940166

5

The impact of single gene and chromosomal disorders on hospital admissions of children and adolescents: a population-based study.

Dye DE, Brameld KJ, Maxwell S, Goldblatt J, Bower C, Leonard H, Bourke J, Glasson EJ, O'Leary P. Dye DE, et al. Public Health Genomics. 2011;14(3):153-61. doi: 10.1159/000321767. Epub 2010 Dec 1. Public Health Genomics. 2011. PMID: 21124008

6

The Western Australian family connections genealogical project: detection of familial occurrences of single gene and chromosomal disorders.

Brameld KJ, Dye DE, Maxwell S, Brisbane JM, Glasson EJ, Goldblatt J, O'Leary P. Brameld KJ, et al. Genet Test Mol Biomarkers. 2014 Feb;18(2):77-82. doi: 10.1089/gtmb.2013.0254. Epub 2014 Jan 9. Genet Test Mol Biomarkers. 2014. PMID: 24405042

7

The triple challenges associated with age-related comorbidities in Down syndrome.

Glasson EJ, Dye DE, Bittles AH. Glasson EJ, et al. Among authors: dye de. J Intellect Disabil Res. 2014 Apr;58(4):393-8. doi: 10.1111/jir.12026. Epub 2013 Mar 19. J Intellect Disabil Res. 2014. PMID: 23510031

8

Mutations and polymorphisms of the skeletal muscle alpha-actin gene (ACTA1).

Laing NG, Dye DE, Wallgren-Pettersson C, Richard G, Monnier N, Lillis S, Winder TL, Lochmüller H, Graziano C, Mitrani-Rosenbaum S, Twomey D, Sparrow JC, Beggs AH, Nowak KJ. Laing NG, et al. Among authors: dye de. Hum Mutat. 2009 Sep;30(9):1267-77. doi: 10.1002/humu.21059. Hum Mutat. 2009. PMID: 19562689 Free PMC article.

9

Congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome: a novel developmental disorder in Gypsies maps to 18qter.

Angelicheva D, Turnev I, Dye D, Chandler D, Thomas PK, Kalaydjieva L. Angelicheva D, et al. Among authors: dye d. Eur J Hum Genet. 1999 Jul;7(5):560-6. doi: 10.1038/sj.ejhg.5200319. Eur J Hum Genet. 1999. PMID: 10439962

10

Actin mutations are one cause of congenital fibre type disproportion.

Laing NG, Clarke NF, Dye DE, Liyanage K, Walker KR, Kobayashi Y, Shimakawa S, Hagiwara T, Ouvrier R, Sparrow JC, Nishino I, North KN, Nonaka I. Laing NG, et al. Ann Neurol. 2004 Nov;56(5):689-94. doi: 10.1002/ana.20260. Ann Neurol. 2004. PMID: 15468086

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