Dye D - Search Results

1

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

2

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

3

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

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

A founder mutation in the GK1 gene is responsible for galactokinase deficiency in Roma (Gypsies).

Kalaydjieva L, Perez-Lezaun A, Angelicheva D, Onengut S, Dye D, Bosshard NU, Jordanova A, Savov A, Yanakiev P, Kremensky I, Radeva B, Hallmayer J, Markov A, Nedkova V, Tournev I, Aneva L, Gitzelmann R. Kalaydjieva L, et al. Among authors: dye d. Am J Hum Genet. 1999 Nov;65(5):1299-307. doi: 10.1086/302611. Am J Hum Genet. 1999. PMID: 10521295 Free PMC article.

7

Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1).

Meredith C, Herrmann R, Parry C, Liyanage K, Dye DE, Durling HJ, Duff RM, Beckman K, de Visser M, van der Graaff MM, Hedera P, Fink JK, Petty EM, Lamont P, Fabian V, Bridges L, Voit T, Mastaglia FL, Laing NG. Meredith C, et al. Am J Hum Genet. 2004 Oct;75(4):703-8. doi: 10.1086/424760. Epub 2004 Aug 20. Am J Hum Genet. 2004. PMID: 15322983 Free PMC article.

8

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

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

The impact of single gene and chromosomal disorders on hospital admissions in an adult population.

Dye DE, Brameld KJ, Maxwell S, Goldblatt J, O'Leary P. Dye DE, et al. J Community Genet. 2011 Jun;2(2):81-90. doi: 10.1007/s12687-011-0043-3. Epub 2011 Mar 2. J Community Genet. 2011. PMID: 22109792 Free PMC article.

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