10 results on '"Rouleau, G.A."'
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2. Evidence for a common ancester in 2 large families with phenotypically variable pastic ataxia
3. Allele Class-independent Intrafamilial correlation of Age at Onset, Age at Hearing Loss and Number of Intracranial Meningiomas in neurofibromatosis 2 (NF2)
4. Krit1 mutations are responsible for the majority of inherited CCMs: a molecular genetic study of 38 families
5. A locus for dominant Hereditary Spastic Ataxia
6. An inducible adenoviral model of OPMD demonstrates time dependent formation of intranuclear inclusions and apoptosis
7. Identification of 20 full-length transcripts in the juvenile amyotrophic lateral sclerosis (ALS2) critical region at chromosome 2q33-q34: Candidate genes for ALS2
8. Polymorphism of the MPO gene in patients with Stroke and Ischemic Hearth Disease
9. The human MJD gene: genomic structure, transcripts, and expression
10. A New Locus for Generalized Epilepsy with Febrile Seizures Plus Maps to Chromosome 2.
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