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Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|April 14, 2005
Anophthalmia and microphthalmia in the Alberta Congenital Anomalies Surveillance SystemR Brian Lowry, Ruth Kohut, Barbara Sibbald, et al.
Clinical Dysmorphology|September 6, 2007
Familial mental retardation due to a cryptic subtelomeric translocation -del 14qter and dup 9qter (the Anyon phenotype)R Brian Lowry, Elizabeth Baker, Joanne Dixon, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 16, 2010
Prevalence of multiple congenital contractures including arthrogryposis multiplex congenita in Alberta, Canada, and a strategy for classification and codingR Brian Lowry, Barbara Sibbald, Tanya Bedard, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|February 14, 2009
Segregation analysis of cleft lip with or without cleft palate in the First Nations (Amerindian) people of British Columbia and review of isolated cleft palate etiologiesR Brian Lowry, Candice Y Johnson, France Gagnon, et al.
American Journal of Medical Genetics. Part A|March 30, 2024
Prenatal findings in 11 cases with craniofacial microsomia using the Alberta Congenital Anomalies Surveillance System, 1997-2019Mary Ann Thomas, Tanya Bedard, Susan Crawford, et al.
The Journal of Hand Surgery|May 6, 2017
Views on the Oberg-Manske-Tonkin Classification System for Congenital Anomalies of the Hand and Upper LimbR Brian Lowry, Tanya Bedard, Gerhard N Kiefer, et al.
Genetics Research International|May 9, 2012
Application of microarray-based comparative genomic hybridization in prenatal and postnatal settings: three case reportsJing Liu, Francois Bernier, Julie Lauzon, et al.
The Journal of Pediatrics|June 2, 2023
Craniofacial Microsomia, Associated Congenital Anomalies, and Risk Factors in 63 Cases from the Alberta Congenital Anomalies Surveillance SystemMary Ann Thomas, Tanya Bedard, Susan Crawford, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 6, 2013
Validation of congenital anomaly coding in Canada's administrative databases compared with a congenital anomaly registryAmy Metcalfe, Barbara Sibbald, R Brian Lowry, et al.
American Journal of Medical Genetics. Part A|May 9, 2007
Absence of PITX2, BARX1, and FOXC1 mutations in De Hauwere syndrome (Axenfeld-Rieger anomaly, hydrocephaly, hearing loss): a 25-year follow upR Brian Lowry, Douglas B Gould, Michael A Walter, et al.
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