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American Journal of Medical Genetics. Part A|November 24, 2017
Congenital limb deficiencies and major associated anomalies in Alberta for the years 1980-2012Tanya Bedard, R Brian Lowry, Barbara Sibbald, et al.
Journal of Registry Management|May 20, 2016
Copy Number Variants and Congenital Anomalies Surveillance: A Suggested Coding Strategy Using the Royal College of Paediatrics and Child Health Version of ICD-10Tanya Bedard, R Brian Lowry, Barbara Sibbald, et al.
Canadian Journal of Public Health = Revue Canadienne De Sante Publique|September 5, 2008
Changes in frequencies of select congenital anomalies since the onset of folic acid fortification in a Canadian birth defect registryKimberly A Godwin, Barbara Sibbald, Tanya Bedard, et al.
American Journal of Medical Genetics. Part A|September 7, 2020
Prevalence rates study of selected isolated non-Mendelian congenital anomalies in the Hutterite population of Alberta, 1980-2016R Brian Lowry, Tanya Bedard, Susan Crawford, et al.
Birth Defects Research|December 19, 2018
Prevalence rates of spina bifida in Alberta, Canada: 2001-2015. Can we achieve more prevention?R Brian Lowry, Tanya Bedard, Amanda J MacFarlane, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|February 5, 2013
Congenital heart defects and major structural noncardiac anomalies in Alberta, Canada, 1995-2002R Brian Lowry, Tanya Bedard, Barbara Sibbald, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|April 5, 2012
Congenital heart defect case ascertainment by the Alberta Congenital Anomalies Surveillance SystemTanya Bedard, R Brian Lowry, Barbara Sibbald, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 6, 2013
Folic acid fortification and the birth prevalence of congenital heart defect cases in Alberta, CanadaTanya Bedard, R Brian Lowry, Barbara Sibbald, et al.
American Journal of Medical Genetics. Part A|October 30, 2007
Newly delineated syndrome of congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE syndrome) in seven patientsJulie C Sapp, Joyce T Turner, Jiddeke M van de Kamp, et al.
American Journal of Medical Genetics. Part A|December 21, 2013
De novo exon 1 missense mutations of SKI and Shprintzen-Goldberg syndrome: two new cases and a clinical reviewP Y Billie Au, Hilary E Racher, John M Graham, et al.
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