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LC Surh

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LC Surh; M Mahadevan; Robert G Korneluk
Analysis of trinucleotide repeats in myotonic dystrophy.
M Cappelli; LC Surh; L Humphreys; S Verma; D Logan; A Hunter; Judith E Allanson
Measuring women's preferences for breast cancer treatments and BRCA1/BRCA2 testing.
M Cappelli; LC Surh; L Humphreys; S Verma; D Logan; A Hunter; Judith E Allanson
Psychological and social determinants of women's decisions to undergo genetic counseling and testing for breast cancer.

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All Publications

2001: LC Surh; M Mahadevan; Robert G Korneluk
Analysis of trinucleotide repeats in myotonic dystrophy.
Current protocols in human genetics / editorial board, Jonathan L. Haines ... [et al.] 2001;Chapter 9():Unit 9.6.
2001: M Cappelli; LC Surh; L Humphreys; S Verma; D Logan; A Hunter; Judith E Allanson
Measuring women's preferences for breast cancer treatments and BRCA1/BRCA2 testing.
Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation 2001;10(7):595-607.
1999: M Cappelli; LC Surh; L Humphreys; S Verma; D Logan; A Hunter; Judith E Allanson
Psychological and social determinants of women's decisions to undergo genetic counseling and testing for breast cancer.
Clinical genetics 1999;55(6):419-30.
1999: R M Frederickson; H S Wang; LC Surh
Some caveats in PCR-based prenatal diagnosis on direct amniotic fluid versus cultured amniocytes.
Prenatal diagnosis 1999;19(2):113-7.
1998: A Hunter; P Wright; M Cappelli; A Kasaboski; LC Surh
Physician knowledge and attitudes towards molecular genetic (DNA) testing of their patients.
Clinical genetics 1998;53(6):447-55.
1997: M Cappelli; LC Surh; S Verma; W Ryan; D Logan; Y Korneluk; David Feeny; A Hunter; Judith E Allanson
Canadian women's attitudes towards breast cancer gene testing.
American journal of human genetics 1997;61(4):A187.
1997: M J Somerville; Alasdair G W Hunter; H L Aubry; Robert G Korneluk; Alex E MacKenzie; LC Surh
Clinical application of the molecular diagnosis of spinal muscular atrophy: deletions of neuronal apoptosis inhibitor protein and survival motor neuron genes.
American journal of medical genetics 1997;69(2):159-65.
1995: Z Yaraghi; M D McLean; N Roy; LC Surh; Joh-E Ikeda; Robert G Korneluk; Alex Mackenzie
A recombination event occurring within two complex 5q13.1 microsatellite repeat polymorphisms suggests a telomeric mapping of spinal muscular atrophy.
Human genetics 1995;96(3):330-4.
1995: LC Surh; P G Wright; M Cappelli; A Kasaboski; V A Hastings; Alasdair G W Hunter
Delivery of molecular genetic services within a health care system: time analysis of the clinical workload. The Molecular Genetic Study Group.
American journal of human genetics 1995;56(3):760-8.
1995: E J Whiting; C Tsilfidis; LC Surh; Alex E MacKenzie; Robert G Korneluk
Convergent myotonic dystrophy (DM) haplotypes: potential inconsistencies in human disease gene localization.
European journal of human genetics : EJHG 1995;3(3):195-202.
1994: M D McLean; N Roy; Alex E MacKenzie; M Salih; Arthur H M Burghes; Louise R Simard; Robert G Korneluk; Joh-E Ikeda; LC Surh
Two 5q13 simple tandem repeat loci are in linkage disequilibrium with type 1 spinal muscular atrophy.
Human molecular genetics 1994;3(11):1951-6.
1994: LC Surh; M Cappelli; N E MacDonald; G Mettler; R E Dales
Cystic fibrosis carrier screening in a high-risk population. Participation based on a traditional recruitment process.
Archives of pediatrics & adolescent medicine 1994;148(6):632-7.
1994: Arthur H M Burghes; S E Ingraham; M McLean; T G Thompson; J D McPherson; Z Kote-Jarai; J D Carpten; CJ DiDonato; Joh-E Ikeda; LC Surh
A multicopy dinucleotide marker that maps close to the spinal muscular atrophy gene.
Genomics 1994;21(2):394-402.
1994: Alex E MacKenzie; P Jacob; LC Surh; A Besner
Genetic heterogeneity in spinal muscular atrophy: a linkage analysis-based assessment.
Neurology 1994;44(5):919-24.
1993: L A Sabouri; M S Mahadevan; Monica Narang; D S Lee; LC Surh; Robert G Korneluk
Effect of the myotonic dystrophy (DM) mutation on mRNA levels of the DM gene.
Nature genetics 1993;4(3):233-8.
1993: M S Mahadevan; M A Foitzik; LC Surh; Robert G Korneluk
Characterization and polymerase chain reaction (PCR) detection of an Alu deletion polymorphism in total linkage disequilibrium with myotonic dystrophy.
Genomics 1993;15(2):446-8.
1993: Alex Mackenzie; N Roy; A Besner; G Mettler; P Jacob; Robert G Korneluk; LC Surh
Genetic linkage analysis of Canadian spinal muscular atrophy kindreds using flanking microsatellite 5q13 polymorphisms.
Human genetics 1993;90(5):501-4.
1992: A Hunter; C Tsilfidis; G Mettler; P Jacob; M Mahadevan; LC Surh; Robert G Korneluk
The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy.
Journal of medical genetics 1992;29(11):774-9.
1991: LC Surh; G G Shutler; Robert G Korneluk
Simple, rapid detection of PCR heteroduplexes in DNA mutations and polymorphisms.
Clinical chemistry 1991;37(12):2142.
1991: Robert G Korneluk; C Tsilfidis; G Shutler; M Mahadevan; J Bailly; LC Surh
A three allele insertion polymorphism is identified by the human chromosome 19q13.3 probe pKBE0.8 (D19S119).
Nucleic acids research 1991;19(5):1157.