Korneluk RG - Search Results

1

Reduction in size of the myotonic dystrophy trinucleotide repeat mutation during transmission.

O'Hoy KL, Tsilfidis C, Mahadevan MS, Neville CE, Barceló J, Hunter AG, Korneluk RG. O'Hoy KL, et al. Among authors: korneluk rg. Science. 1993 Feb 5;259(5096):809-12. doi: 10.1126/science.8094260. Science. 1993. PMID: 8094260

2

The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy.

Hunter A, Tsilfidis C, Mettler G, Jacob P, Mahadevan M, Surh L, Korneluk R. Hunter A, et al. J Med Genet. 1992 Nov;29(11):774-9. doi: 10.1136/jmg.29.11.774. J Med Genet. 1992. PMID: 1453425 Free PMC article.

3

Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy.

Tsilfidis C, MacKenzie AE, Mettler G, Barceló J, Korneluk RG. Tsilfidis C, et al. Among authors: korneluk rg. Nat Genet. 1992 Jun;1(3):192-5. doi: 10.1038/ng0692-192. Nat Genet. 1992. PMID: 1303233

4

Physical mapping and cloning of the proximal segment of the myotonic dystrophy gene region.

Shutler G, Korneluk RG, Tsilfidis C, Mahadevan M, Bailly J, Smeets H, Jansen G, Wieringa B, Lohman F, Aslanidis C, et al. Shutler G, et al. Among authors: korneluk rg. Genomics. 1992 Jul;13(3):518-25. doi: 10.1016/0888-7543(92)90119-d. Genomics. 1992. PMID: 1639380

5

Linkage analysis of the apolipoprotein C2 gene and myotonic dystrophy on human chromosome 19 reveals linkage disequilibrium in a French-Canadian population.

MacKenzie AE, MacLeod HL, Hunter AG, Korneluk RG. MacKenzie AE, et al. Among authors: korneluk rg. Am J Hum Genet. 1989 Jan;44(1):140-7. Am J Hum Genet. 1989. PMID: 2562820 Free PMC article.

6

Convergent myotonic dystrophy (DM) haplotypes: potential inconsistencies in human disease gene localization.

Whiting EJ, Tsilfidis C, Surh L, MacKenzie AE, Korneluk RG. Whiting EJ, et al. Among authors: korneluk rg. Eur J Hum Genet. 1995;3(3):195-202. doi: 10.1159/000472295. Eur J Hum Genet. 1995. PMID: 7583045

7

High resolution genetic analysis suggests one ancestral predisposing haplotype for the origin of the myotonic dystrophy mutation.

Neville CE, Mahadevan MS, Barceló JM, Korneluk RG. Neville CE, et al. Among authors: korneluk rg. Hum Mol Genet. 1994 Jan;3(1):45-51. doi: 10.1093/hmg/3.1.45. Hum Mol Genet. 1994. PMID: 7909252

8

Intergenerational stability of the myotonic dystrophy protomutation.

Barceló JM, Mahadevan MS, Tsilfidis C, MacKenzie AE, Korneluk RG. Barceló JM, et al. Among authors: korneluk rg. Hum Mol Genet. 1993 Jun;2(6):705-9. doi: 10.1093/hmg/2.6.705. Hum Mol Genet. 1993. PMID: 8353489

9

Effect of the myotonic dystrophy (DM) mutation on mRNA levels of the DM gene.

Sabouri LA, Mahadevan MS, Narang M, Lee DS, Surh LC, Korneluk RG. Sabouri LA, et al. Among authors: korneluk rg. Nat Genet. 1993 Jul;4(3):233-8. doi: 10.1038/ng0793-233. Nat Genet. 1993. PMID: 8358430

10

Decrease in the size of the myotonic dystrophy CTG repeat during transmission from parent to child: implications for genetic counselling and genetic anticipation.

Hunter AG, Jacob P, O'Hoy K, MacDonald I, Mettler G, Tsilfidis C, Korneluk RG. Hunter AG, et al. Among authors: korneluk rg. Am J Med Genet. 1993 Feb 1;45(3):401-7. doi: 10.1002/ajmg.1320450330. Am J Med Genet. 1993. PMID: 8434633

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

174 results

Search Page

Filters