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Selective Oxidation of Glycerol to Dihydroxyacetone over Pt−Bi/C Catalyst: Optimization of Catalyst and Reaction Conditions

Industrial & engineering chemistry research, 2010-11, Vol.49 (21), p.10876-10882

2010

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Reduction in Neural-Tube Defects after Folic Acid Fortification in Canada

The New England journal of medicine, 2007-07, Vol.357 (2), p.135-142

2007

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Mutations in BICD2, which Encodes a Golgin and Important Motor Adaptor, Cause Congenital Autosomal-Dominant Spinal Muscular Atrophy

American journal of human genetics, 2013-06, Vol.92 (6), p.946-954

2013

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Kinetic study of glycerol oxidation network over Pt–Bi/C catalyst

Applied catalysis. B, Environmental, 2011-07, Vol.106 (1-2), p.123-132

2011

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Reprogramming a module of the 6-deoxyerythronolide B synthase for iterative chain elongation

Proceedings of the National Academy of Sciences - PNAS, 2012-03, Vol.109 (11), p.4110-4115

2012

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Newly delineated syndrome of congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE syndrome) in seven patients

American journal of medical genetics. Part A, 2007-12, Vol.143A (24), p.2944-2958

2007

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Craniofacial Microsomia, Associated Congenital Anomalies, and Risk Factors in 63 Cases from the Alberta Congenital Anomalies Surveillance System

The Journal of pediatrics, 2023-10, Vol.261, p.113528-113528, Article 113528

2023

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The Alberta Congenital Anomalies Surveillance System: a 40-year review with prevalence and trends for selected congenital anomalies, 1997-2019

Health promotion and chronic disease prevention in Canada, 2023-01, Vol.43 (1), p.40-48

2023

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Conjoined twins: A worldwide collaborative epidemiological study of the International Clearinghouse for Birth Defects Surveillance and Research

American journal of medical genetics. Part C, Seminars in medical genetics, 2011-11, Vol.157C (4), p.274-287

2011

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Risk Assessment of the Leachables’ Profile for Small-Molecule Pharmaceutical Drug Substances

Organic process research & development, 2021-12, Vol.25 (12), p.2693-2706

2021

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Views on the Oberg-Manske-Tonkin Classification System for Congenital Anomalies of the Hand and Upper Limb

The Journal of hand surgery (American ed.), 2017-05, Vol.42 (5), p.378-381

2017

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A Turnstile Mechanism for the Controlled Growth of Biosynthetic Intermediates on Assembly Line Polyketide Synthases

ACS central science, 2016-01, Vol.2 (1), p.14-20

2016

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Prenatal findings in 11 cases with craniofacial microsomia using the Alberta Congenital Anomalies Surveillance System, 1997–2019

American journal of medical genetics. Part A, 2024-08, Vol.194 (8), p.e63594-n/a

2024

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Disease coding systems for arthrogryposis multiplex congenita

American journal of medical genetics. Part C, Seminars in medical genetics, 2019-09, Vol.181 (3), p.304-309

2019

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Bladder exstrophy: An epidemiologic study from the International Clearinghouse for Birth Defects Surveillance and Research, and an overview of the literature

American journal of medical genetics. Part C, Seminars in medical genetics, 2011-11, Vol.157C (4), p.321-332

2011

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Congenital limb deficiencies in Alberta-a review of 33 years (1980-2012) from the Alberta Congenital Anomalies Surveillance System (ACASS)

American journal of medical genetics. Part A, 2015-11, Vol.167A (11), p.2599-2609

2015

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Cloacal exstrophy: An epidemiologic study from the International Clearinghouse for Birth Defects Surveillance and Research

American journal of medical genetics. Part C, Seminars in medical genetics, 2011-11, Vol.157C (4), p.333-343

2011

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Gastroschisis and associated defects: An international study

American journal of medical genetics. Part A, 2007-04, Vol.143A (7), p.660-671

2007

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Heterologous expression of diverse propionyl-CoA carboxylases affects polyketide production in Escherichia coli

Journal of antibiotics, 2017-07, Vol.70 (7), p.859-863

2017

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Axenfeld-Rieger syndrome: more than meets the eye

Journal of medical genetics, 2023-04, Vol.60 (4), p.368

2023

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Prevalence of multiple congenital contractures including arthrogryposis multiplex congenita in Alberta, Canada, and a strategy for classification and coding

Birth defects research. A Clinical and molecular teratology, 2010-12, Vol.88 (12), p.1057-1061

2010

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Hypospadias Prevalence and Trends in International Birth Defect Surveillance Systems, 1980–2010

European urology, 2019-10, Vol.76 (4), p.482-490

2019

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Triple surveillance: The future for birth defect registries

European journal of medical genetics, 2019-09, Vol.62 (9), p.103553-103553, Article 103553

2019

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GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype

Human mutation, 2009-05, Vol.30 (5), p.724-733

2009

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Trends of selected malformations in relation to folic acid recommendations and fortification: An international assessment

Birth defects research. A Clinical and molecular teratology, 2006-10, Vol.76 (10), p.693-705

2006

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Selective Oxidation of Glycerol to Dihydroxyacetone over Pt−Bi/C Catalyst: Optimization of Catalyst and Reaction Conditions

Reduction in Neural-Tube Defects after Folic Acid Fortification in Canada

Mutations in BICD2, which Encodes a Golgin and Important Motor Adaptor, Cause Congenital Autosomal-Dominant Spinal Muscular Atrophy

Kinetic study of glycerol oxidation network over Pt–Bi/C catalyst

Reprogramming a module of the 6-deoxyerythronolide B synthase for iterative chain elongation

Newly delineated syndrome of congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE syndrome) in seven patients

Craniofacial Microsomia, Associated Congenital Anomalies, and Risk Factors in 63 Cases from the Alberta Congenital Anomalies Surveillance System

The Alberta Congenital Anomalies Surveillance System: a 40-year review with prevalence and trends for selected congenital anomalies, 1997-2019

Conjoined twins: A worldwide collaborative epidemiological study of the International Clearinghouse for Birth Defects Surveillance and Research

Risk Assessment of the Leachables’ Profile for Small-Molecule Pharmaceutical Drug Substances

Views on the Oberg-Manske-Tonkin Classification System for Congenital Anomalies of the Hand and Upper Limb

A Turnstile Mechanism for the Controlled Growth of Biosynthetic Intermediates on Assembly Line Polyketide Synthases

Prenatal findings in 11 cases with craniofacial microsomia using the Alberta Congenital Anomalies Surveillance System, 1997–2019

Disease coding systems for arthrogryposis multiplex congenita

Bladder exstrophy: An epidemiologic study from the International Clearinghouse for Birth Defects Surveillance and Research, and an overview of the literature

Congenital limb deficiencies in Alberta-a review of 33 years (1980-2012) from the Alberta Congenital Anomalies Surveillance System (ACASS)

Cloacal exstrophy: An epidemiologic study from the International Clearinghouse for Birth Defects Surveillance and Research

Gastroschisis and associated defects: An international study

Heterologous expression of diverse propionyl-CoA carboxylases affects polyketide production in Escherichia coli

Axenfeld-Rieger syndrome: more than meets the eye

Prevalence of multiple congenital contractures including arthrogryposis multiplex congenita in Alberta, Canada, and a strategy for classification and coding

Hypospadias Prevalence and Trends in International Birth Defect Surveillance Systems, 1980–2010

Triple surveillance: The future for birth defect registries

GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype

Trends of selected malformations in relation to folic acid recommendations and fortification: An international assessment

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