Korneluk RG - Search Results

1

Clinical application of the molecular diagnosis of spinal muscular atrophy: deletions of neuronal apoptosis inhibitor protein and survival motor neuron genes.

Somerville MJ, Hunter AG, Aubry HL, Korneluk RG, MacKenzie AE, Surh LC. Somerville MJ, et al. Among authors: korneluk rg. Am J Med Genet. 1997 Mar 17;69(2):159-65. Am J Med Genet. 1997. PMID: 9056553

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

Genetic linkage analysis of Canadian spinal muscular atrophy kindreds using flanking microsatellite 5q13 polymorphisms.

MacKenzie A, Roy N, Besner A, Mettler G, Jacob P, Korneluk R, Surh L. MacKenzie A, et al. Hum Genet. 1993 Jan;90(5):501-4. doi: 10.1007/BF00217448. Hum Genet. 1993. PMID: 8094064

4

A recombination event occurring within two complex 5q13.1 microsatellite repeat polymorphisms suggests a telomeric mapping of spinal muscular atrophy.

Yaraghi Z, McLean MD, Roy N, Surh L, Ikeda JE, Korneluk RG, MacKenzie A. Yaraghi Z, et al. Among authors: korneluk rg. Hum Genet. 1995 Sep;96(3):330-4. doi: 10.1007/BF00210417. Hum Genet. 1995. PMID: 7649551

5

Two 5q13 simple tandem repeat loci are in linkage disequilibrium with type 1 spinal muscular atrophy.

McLean MD, Roy N, MacKenzie AE, Salih M, Burghes AH, Simard L, Korneluk RG, Ikeda JE, Surh L. McLean MD, et al. Among authors: korneluk rg. Hum Mol Genet. 1994 Nov;3(11):1951-6. doi: 10.1093/hmg/3.11.1951. Hum Mol Genet. 1994. PMID: 7874111

6

FISH detection of chromosome polymorphism and deletions in the spinal muscular atrophy (SMA) region of 5q13.

Rajcan-Separovic E, Mahadevan MS, Lefebvre C, Besner-Johnston A, Ikeda JE, Korneluk RG, MacKenzie A. Rajcan-Separovic E, et al. Among authors: korneluk rg. Cytogenet Cell Genet. 1996;75(4):243-7. doi: 10.1159/000134493. Cytogenet Cell Genet. 1996. PMID: 9067434

7

Sequence of a 131-kb region of 5q13.1 containing the spinal muscular atrophy candidate genes SMN and NAIP.

Chen Q, Baird SD, Mahadevan M, Besner-Johnston A, Farahani R, Xuan J, Kang X, Lefebvre C, Ikeda JE, Korneluk RG, MacKenzie AE. Chen Q, et al. Among authors: korneluk rg. Genomics. 1998 Feb 15;48(1):121-7. doi: 10.1006/geno.1997.5141. Genomics. 1998. PMID: 9503025

8

Cloning and characterization of the multiple murine homologues of NAIP (neuronal apoptosis inhibitory protein).

Yaraghi Z, Korneluk RG, MacKenzie A. Yaraghi Z, et al. Among authors: korneluk rg. Genomics. 1998 Jul 1;51(1):107-13. doi: 10.1006/geno.1998.5378. Genomics. 1998. PMID: 9693038

9

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

10

Simple, rapid detection of PCR heteroduplexes in DNA mutations and polymorphisms.

Surh LC, Shutler GG, Korneluk RG. Surh LC, et al. Among authors: korneluk rg. Clin Chem. 1991 Dec;37(12):2142. Clin Chem. 1991. PMID: 1764797 No abstract available.

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