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Author/Creator Majewski, J

1. B.06 Whole exome sequencing in genetic ataxias associated with cerebellar atrophy: the Canadian experience. (5th June 2019)

Authors:
Gauquelin, L; Hartley, T; Tarnopolsky, M; Dyment, DA; Brais, B; Geraghty, MT; Tétreault, M; Ahmed, S; Rojas, S; Majewski, J; Bernier, F; Innes, A; Rouleau, G; Suchowersky, O; Boycott, KM; Yoon, G
Journal:
Canadian journal of neurological sciences
Issue:
Volume 46(2019)Supplement 1
Page Start:
S11
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. B.06 Whole exome sequencing in genetic ataxias associated with cerebellar atrophy: the Canadian experience. (June 2019)

Authors:
Gauquelin, L; Hartley, T; Tarnopolsky, M; Dyment, DA; Brais, B; Geraghty, MT; Tétreault, M; Ahmed, S; Rojas, S; Majewski, J; Bernier, F; Innes, A; Rouleau, G; Suchowersky, O; Boycott, KM; Yoon, G
Journal:
Canadian journal of neurological sciences
Issue:
Volume 46(2019)Supplement 1
Page Start:
S11
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. WDR19: An ancient, retrograde, intraflagellar ciliary protein is mutated in autosomal recessive retinitis pigmentosa and in Senior‐Loken syndrome. (9th July 2013)

Authors:
Coussa, R G; Otto, E A; Gee, H‐Y; Arthurs, P; Ren, H; Lopez, I; Keser, V; Fu, Q; Faingold, R; Khan, A; Schwartzentruber, J; Majewski, J; Hildebrandt, F; Koenekoop, R K
Journal:
Clinical genetics
Issue:
Volume 84:Number 2(2013:Aug.)
Page Start:
150
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗