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Author/Creator Horvath, G.A.

1. Debunking Occam's razor: Diagnosing multiple genetic diseases in families by whole‐exome sequencing. Issue 3 (13th March 2017)

Authors:
Balci, T.B.; Hartley, T.; Xi, Y.; Dyment, D.A.; Beaulieu, C.L.; Bernier, F.P.; Dupuis, L.; Horvath, G.A.; Mendoza‐Londono, R.; Prasad, C.; Richer, J.; Yang, X.‐R.; Armour, C.M.; Bareke, E.; Fernandez, B.A.; McMillan, H.J.; Lamont, R.E.; Majewski, J.; Parboosingh, J.S.; Prasad, A.N.
Journal:
Clinical genetics
Issue:
Volume 92:Issue 3(2017)
Page Start:
281
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Whole‐exome sequencing is a valuable diagnostic tool for inherited peripheral neuropathies: Outcomes from a cohort of 50 families. Issue 2 (12th December 2017)

Authors:
Hartley, T.; Wagner, J.D.; Warman‐Chardon, J.; Tétreault, M.; Brady, L.; Baker, S.; Tarnopolsky, M.; Bourque, P.R.; Parboosingh, J.S.; Smith, C.; McInnes, B.; Innes, A.M.; Bernier, F.; Curry, C.J.; Yoon, G.; Horvath, G.A.; Bareke, E.; Gillespie, M.; Majewski, J.; Bulman, D.E.
Journal:
Clinical genetics
Issue:
Volume 93:Issue 2(2018)
Page Start:
301
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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