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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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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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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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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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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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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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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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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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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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The hutterite variant of treacher collins syndrome: A 28-year-old story solved

American journal of medical genetics. Part A, 2013-11, Vol.161A (11), p.2855-2859

2013

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Orofacial clefts in California: No decline in Alberta, Canada

American journal of medical genetics. Part A, 2019-06, Vol.179 (6), p.1077-1079

2019

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Phenotype and pathology of the dilated cardiomyopathy with ataxia syndrome in children

Journal of inherited metabolic disease, 2022-03, Vol.45 (2), p.366-376

2022

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Cyclopia: An epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research

American journal of medical genetics. Part C, Seminars in medical genetics, 2011-11, Vol.157C (4), p.344-357

2011

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Incidence of inborn errors of metabolism in British Columbia, 1969-1996

Pediatrics (Evanston), 2000-01, Vol.105 (1), p.e10

2000

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Prevalence rates study of selected isolated non‐Mendelian congenital anomalies in the Hutterite population of Alberta, 1980–2016

American journal of medical genetics. Part A, 2020-11, Vol.182 (11), p.2594-2604

2020

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PITX2 and FOXC1 spectrum of mutations in ocular syndromes

European journal of human genetics : EJHG, 2012-12, Vol.20 (12), p.1224-1233

2012

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Acardia: Epidemiologic findings and literature review 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.262-273

2011

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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

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

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

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

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

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

Gastroschisis and associated defects: An international study

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

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

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

The hutterite variant of treacher collins syndrome: A 28-year-old story solved

Orofacial clefts in California: No decline in Alberta, Canada

Phenotype and pathology of the dilated cardiomyopathy with ataxia syndrome in children

Cyclopia: An epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research

Incidence of inborn errors of metabolism in British Columbia, 1969-1996

Prevalence rates study of selected isolated non‐Mendelian congenital anomalies in the Hutterite population of Alberta, 1980–2016

PITX2 and FOXC1 spectrum of mutations in ocular syndromes

Acardia: Epidemiologic findings and literature review from the International Clearinghouse for Birth Defects Surveillance and Research

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