Reply to Kock et al.

por Desautels, A., Turecki, G., Montplaisir, J., Rouleau, G. A.
Publicado 2002

Ambulatory Goeckerman treatment of psoriasis: experience with 200 patients.

por DesGroseilliers, J P, Cullen, A E, Rouleau, G A
Publicado 1981

Mosaicism of the CAG repeat in CNS tissue in relation to age at death in spinocerebellar ataxia type 1 and Machado-Joseph disease patients.

por Maciel, P, Lopes-Cendes, I, Kish, S, Sequeiros, J, Rouleau, G A
Publicado 1997

Dinucleotide repeat polymorphism at the IGF2R locus

por Goto, J., Figlewicz, D.A., Marineau, C., Khodr, N., Rouleau, G.A.
Publicado 1992

A Pvull RFLP at the HOX 1.4 homeobox locus (HOX1D)

por Goto, J., Figlewicz, D.A., Lutchman, M., Ruddle, F., Rouleau, G.A.
Publicado 1991

Gamma-glutamyl transferase locus (GGT) displays a PvuII polymorphism.

por Rouleau, G A, Bazanowski, A, Cohen, E H, Guellaen, G, Gusella, J F
Publicado 1988

A New Locus for Generalized Epilepsy with Febrile Seizures Plus Maps to Chromosome 2

por Lopes-Cendes, I., Scheffer, I. E., Berkovic, S. F., Rousseau, M., Andermann, E., Rouleau, G. A.
Publicado 2000

FAMILIAL CONGENITAL MIRROR MOVEMENTS: REPORT OF A LARGE 4-GENERATION FAMILY

por Srour, M, Philibert, M, Dion, M -H., Duquette, A, Richer, F, Rouleau, G A., Chouinard, S
Publicado 2009

D22S15--a fetal brain cDNA with BanII and SacI RFLP.

por Rouleau, G A, Kurnit, D M, Neve, R L, Bazanowsky, A, Patterson, D, Gusella, J F
Publicado 1988

Parental origin of chromosome 22 alleles lost in meningioma.

por Sanson, M, Delattre, O, Couturier, J, Philippon, J, Cophignon, J, Derome, P, Rouleau, G A, Thomas, G
Publicado 1990

A Locus for Autosomal Dominant Hereditary Spastic Ataxia, SAX1, Maps to Chromosome 12p13

por Meijer, I. A., Hand, C. K., Grewal, K. K., Stefanelli, M. G., Ives, E. J., Rouleau, G. A.
Publicado 2002

Linkage analysis of the nail-patella syndrome.

por Campeau, E, Watkins, D, Rouleau, G A, Babul, R, Buchanan, J A, Meschino, W, Der Kaloustian, V M
Publicado 1995

Equal parental origin of chromosome 22 losses in human sporadic meningioma: no evidence for genomic imprinting.

por Fontaine, B, Rouleau, G A, Seizinger, B, Jewell, A F, Hanson, M P, Martuza, R L, Gusella, J F
Publicado 1990

Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate region.

por Lopes-Cendes, I., Andermann, E., Attig, E., Cendes, F., Bosch, S., Wagner, M., Gerstenbrand, F., Andermann, F., Rouleau, G. A.
Publicado 1994

Lithium chloride attenuates cell death in oculopharyngeal muscular dystrophy by perturbing Wnt/β-catenin pathway

por Abu-Baker, A, Laganiere, J, Gaudet, R, Rochefort, D, Brais, B, Neri, C, Dion, P A, Rouleau, G A
Publicado 2013

Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22.

por Rouleau, G A, Seizinger, B R, Wertelecki, W, Haines, J L, Superneau, D W, Martuza, R L, Gusella, J F
Publicado 1990

A new locus for autosomal dominant intracranial aneurysm, ANIB4, maps to chromosome 5p15.2‐14.3

por Verlaan, D J, Dubé, M‐P, St‐Onge, J, Noreau, A, Roussel, J, Satgé, N, Wallace, M C, Rouleau, G A
Publicado 2006

Mutation detection in Machado-Joseph disease using repeat expansion detection.

por Lindblad, K., Lunkes, A., Maciel, P., Stevanin, G., Zander, C., Klockgether, T., Ratzlaff, T., Brice, A., Rouleau, G. A., Hudson, T., Auburger, G., Schalling, M.
Publicado 1996

Hereditary spastic paraplegia: LOD-score considerations for confirmation of linkage in a heterogeneous trait.

por Dubé, M P, Mlodzienski, M A, Kibar, Z, Farlow, M R, Ebers, G, Harper, P, Kolodny, E H, Rouleau, G A, Figlewicz, D A
Publicado 1997

Identification of new mutations in the Cu/Zn superoxide dismutase gene of patients with familial amyotrophic lateral sclerosis.

por Pramatarova, A, Figlewicz, D A, Krizus, A, Han, F Y, Ceballos-Picot, I, Nicole, A, Dib, M, Meininger, V, Brown, R H, Rouleau, G A
Publicado 1995