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Publications by Sylvie Forlani
SCA15 Due to Large ITPR1 Deletions in a Cohort of 333 White Families With Dominant Ataxia
Archives of Neurology
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Analyses of Del(GJB6‐D13S1830) and Del(GJB6‐D13S1834) Deletions in a Large Cohort With Hearing Loss: Caveats to Interpretation of Molecular Test Results in Multiplex Families
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Correction: Mutational Analysis of ITPR1 in a Taiwanese Cohort With Cerebellar Ataxias
PLoS ONE
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Pituitary Responses to a Neuroactive Tripeptide (TRH) in Friedreich’s Ataxia Families
Canadian Journal of Neurological Sciences
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Genomic Mechanisms underlyingPARK2large Deletions Identified in a Cohort of Patients With PD
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Autosomal Dominant Cerebellar Ataxia With Deafness, Myoclonus and Amyotrophy.
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Severe Congenital Cutis Laxa With Cardiovascular Manifestations Due to Homozygous Deletions in ALDH18A1
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Families Coping With Disability Due to Brain Injury in Oman
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Accuracy of Genomic Selection Models in a Large Population of Open-Pollinated Families in White Spruce
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Progressive Ataxia Due to a Missense Mutation in a Calcium-Channel Gene
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