Author: "Rouleau, G.A." / Publisher: university of chicago press - Searchworks@Jio Institute Digital Library Search Results

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Your search keyword '"Rouleau, G.A."' showing total 9 results

Start Over Author "Rouleau, G.A." Publisher university of chicago press

9 results on '"Rouleau, G.A."'

1. A locus for autosomal dominant hereditary spastic ataxia, SAX1, maps to chromosome 12p13

Author: Meijer, I.A., Hand, C.K., Grewal, K.K., Stefanelli, M.G., Ives, E.J., and Rouleau, G.A.
Subjects: Ataxia -- Genetic aspects, Genetic disorders -- Research, Biological sciences
Published: 2002

2. Evidence for a common ancester in 2 large families with phenotypically variable pastic ataxia

Author: Grewal, K.K., Stefanelli, M.G., Meijer, I.A., Hand, C.K., Rouleau, G.A., and Ives, E.J.
Subjects: Human genetics -- Research, Nervous system -- Degeneration, Ataxia -- Genetic aspects, Spasticity -- Genetic aspects, Biological sciences
Published: 2001

3. Allele Class-independent Intrafamilial correlation of Age at Onset, Age at Hearing Loss and Number of Intracranial Meningiomas in neurofibromatosis 2 (NF2)

Author: Zhao, Y., Kumar, R.A., Baser, M.E., Evans, D.G.R., Wallace, A., Rouleau, G.A., Mautner, V.F., Kluwe, L., Joe, H., and Friedman, J.M.
Subjects: Genetic disorders -- Research, Neurofibromatosis -- Physiological aspects, Human genetics -- Research, Biological sciences
Published: 2001

4. Krit1 mutations are responsible for the majority of inherited CCMs: a molecular genetic study of 38 families

Author: Verlaan, D., Davenport, W.J., Stefan, H., Siegel, A.M., and Rouleau, G.A.
Subjects: Human genetics -- Research, Genetic disorders -- Research, Brain diseases -- Diseases, Hemorrhagic diseases -- Genetic aspects, Biological sciences
Published: 2001

5. A locus for dominant Hereditary Spastic Ataxia

Author: Meijer, I.A., Hand, C.K., Grewal, K.K., Stefanelli, M.G., Ives, E.J., and Rouleau, G.A.
Subjects: Human genetics -- Research, Nervous system -- Degeneration, Genetic disorders -- Research, Biological sciences
Published: 2001

6. An inducible adenoviral model of OPMD demonstrates time dependent formation of intranuclear inclusions and apoptosis

Author: Lavoie, H., Dicaire, M-J., Denis, S., Rouleau, G.A., Massie, B., Langelier, Y., and Brais, B.
Subjects: Genetic research -- Analysis, Human genetics -- Research, Muscular dystrophy -- Genetic aspects, Biological sciences
Published: 2000

7. Identification of 20 full-length transcripts in the juvenile amyotrophic lateral sclerosis (ALS2) critical region at chromosome 2q33-q34: Candidate genes for ALS2

Author: Hadano, S., Yanagisawa, Y., Skaug, J., Fichter, K., Scherer, S.W., Rouleau, G.A., Hayden, M.R., and Ikeda, J.-E.
Subjects: Genetic research -- Analysis, Human genetics -- Research, Sclerosis -- Genetic aspects, Biological sciences
Published: 2000

8. Polymorphism of the MPO gene in patients with Stroke and Ischemic Hearth Disease

Author: Nikpoor, B. and Rouleau, G.A.
Subjects: Human genetics -- Research, Atherosclerosis -- Genetic aspects, Biological sciences
Published: 2000

9. The human MJD gene: genomic structure, transcripts, and expression

Author: Ichikawa, Y., Goto, J., Hattori, M., Toyoda, A., Ishii, K., Jeong, S.-Y., Hashida, H., Masuda, N., Ogata, K., Suzuki, Y., Sugano, S., Kasai, F., Hirai, M., Maciel, P., Rouleau, G.A., Sakaki, Y., and Kanazawa, I.
Subjects: Genetic research -- Analysis, Human genetics -- Research, Cerebellar ataxia -- Genetic aspects, Biological sciences
Published: 2000

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