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Birth Defects Research|January 5, 2024
Publicly funded healthcare costs associated with orofacial clefts for children born in Alberta, Canada between 2002 and 2018Tanya Bedard, R Brian Lowry, Susan Crawford, et al.
Journal of Inherited Metabolic Disease|September 28, 2021
Phenotype and pathology of the dilated cardiomyopathy with ataxia syndrome in childrenPranav Machiraju, Vlad Degtiarev, Dhwani Patel, et al.
Health Promotion and Chronic Disease Prevention in Canada : Research, Policy and Practice|January 18, 2023
The Alberta Congenital Anomalies Surveillance System: a 40-year review with prevalence and trends for selected congenital anomalies, 1997-2019R Brian Lowry, Tanya Bedard, Xin Grevers, et al.
Human Mutation|April 2, 2009
GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotypeWilliam A Paznekas, Barbara Karczeski, Sascha Vermeer, et al.
European Journal of Human Genetics : EJHG|May 10, 2012
PITX2 and FOXC1 spectrum of mutations in ocular syndromesLinda M Reis, Rebecca C Tyler, Bethany A Volkmann Kloss, et al.
American Journal of Medical Genetics. Part A|March 19, 2008
Clinical genetics and the Hutterite population: a review of Mendelian disordersKym M Boycott, Jillian S Parboosingh, Bernie N Chodirker, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 1, 2007
Impact of folic acid food fortification on the birth prevalence of lipomyelomeningocele in CanadaPhilippe De Wals, Margot I Van Allen, R Brian Lowry, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|July 26, 2008
Spina bifida before and after folic acid fortification in CanadaPhilippe De Wals, Fassiatou Tairou, Margot I Van Allen, et al.
The New England Journal of Medicine|July 13, 2007
Reduction in neural-tube defects after folic acid fortification in CanadaPhilippe De Wals, Fassiatou Tairou, Margot I Van Allen, et al.
Human Mutation|August 10, 2005
SALL1 mutation analysis in Townes-Brocks syndrome: twelve novel mutations and expansion of the phenotypeElke M Botzenhart, Andrew Green, Helena Ilyina, et al.
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