Surh L - Search Results

1

A multicopy dinucleotide marker that maps close to the spinal muscular atrophy gene.

Burghes AH, Ingraham SE, McLean M, Thompson TG, McPherson JD, Kote-Jarai Z, Carpten JD, DiDonato CJ, Ikeda JE, Surh L, et al. Burghes AH, et al. Among authors: surh l. Genomics. 1994 May 15;21(2):394-402. doi: 10.1006/geno.1994.1282. Genomics. 1994. PMID: 8088834

2

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: surh l. Hum Genet. 1995 Sep;96(3):330-4. doi: 10.1007/BF00210417. Hum Genet. 1995. PMID: 7649551

3

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: surh l. Hum Mol Genet. 1994 Nov;3(11):1951-6. doi: 10.1093/hmg/3.11.1951. Hum Mol Genet. 1994. PMID: 7874111

4

Molecular diagnosis of non-deletion SMA patients using quantitative PCR of SMN exon 7.

Rochette CF, Surh LC, Ray PN, McAndrew PE, Prior TW, Burghes AH, Vanasse M, Simard LR. Rochette CF, et al. Among authors: surh lc. Neurogenetics. 1997 Sep;1(2):141-7. doi: 10.1007/s100480050021. Neurogenetics. 1997. PMID: 10732817

5

Characterization and polymerase chain reaction (PCR) detection of an Alu deletion polymorphism in total linkage disequilibrium with myotonic dystrophy.

Mahadevan MS, Foitzik MA, Surh LC, Korneluk RG. Mahadevan MS, et al. Among authors: surh lc. Genomics. 1993 Feb;15(2):446-8. doi: 10.1006/geno.1993.1087. Genomics. 1993. PMID: 8449517

6

Genetic heterogeneity in spinal muscular atrophy: a linkage analysis-based assessment.

MacKenzie AE, Jacob P, Surh L, Besner A. MacKenzie AE, et al. Among authors: surh l. Neurology. 1994 May;44(5):919-24. doi: 10.1212/wnl.44.5.919. Neurology. 1994. PMID: 8190297

7

Assignment of the structural gene for argininosuccinate synthetase to proximal mouse chromosome 2.

Jackson MJ, Surh LC, O'Brien WE, Beaudet AL. Jackson MJ, et al. Among authors: surh lc. Genomics. 1990 Mar;6(3):545-7. doi: 10.1016/0888-7543(90)90484-c. Genomics. 1990. PMID: 1970331

8

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. Among authors: surh l. Hum Genet. 1993 Jan;90(5):501-4. doi: 10.1007/BF00217448. Hum Genet. 1993. PMID: 8094064

9

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: surh lc. Am J Med Genet. 1997 Mar 17;69(2):159-65. Am J Med Genet. 1997. PMID: 9056553

10

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: surh l. Eur J Hum Genet. 1995;3(3):195-202. doi: 10.1159/000472295. Eur J Hum Genet. 1995. PMID: 7583045

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