about
Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGHRace and ancestry in biomedical research: exploring the challengesMutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosisThe gene for juvenile hyaline fibromatosis maps to chromosome 4q21The shared pathoetiological effects of particulate air pollution and the social environment on fetal-placental developmentCarnitine palmitoyltransferase 1A (CPT1A) P479L prevalence in live newborns in Yukon, Northwest Territories, and NunavutEvidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12–q21Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization.Heavy smoking during pregnancy as a marker for other risk factors of adverse birth outcomes: a population-based study in British Columbia, Canada.Recognizing life-threatening causes of syncope.The Canadian Arrhythmogenic Right Ventricular Cardiomyopathy Registry: Rationale, Design, and Preliminary Recruitment.Novel Variant in the ANK2 Membrane-Binding Domain Is Associated With Ankyrin-B Syndrome and Structural Heart Disease in a First Nations Population With a High Rate of Long QT Syndrome.Genetic Testing in the Evaluation of Unexplained Cardiac Arrest: From the CASPER (Cardiac Arrest Survivors With Preserved Ejection Fraction Registry).Autoimmune liver disease and the Canadian First Nations Aboriginal Communities of British Columbia's Pacific Northwest.KCNQ1 p.L353L affects splicing and modifies the phenotype in a founder population with long QT syndrome type 1.Hypomorphic temperature-sensitive alleles of NSDHL cause CK syndromeCauses and risk factors for infant mortality in Nunavut, Canada 1999-2011Oligonucleotide microarray analysis of genomic imbalance in children with mental retardationHeart defects and other malformations in the Inuit in Canada: a baseline study.Characteristics of primary biliary cirrhosis in British Columbia's First Nations population.Air pollution, neighbourhood and maternal-level factors modify the effect of smoking on birth weight: a multilevel analysis in British Columbia, Canada.DNA on loan: issues to consider when carrying out genetic research with aboriginal families and communities.The reduction of birth weight by fine particulate matter and its modification by maternal and neighbourhood-level factors: a multilevel analysis in British Columbia, CanadaRetrospective review of pediatric and adult autoimmune hepatitis in two quaternary care centres in British Columbia: increased prevalence seen in British Columbia's First Nations community.The current state of birth outcome and birth defect surveillance in northern regions of the world.Inherited heart rhythm disease: negotiating the minefield for the practicing cardiologist.Congenital microcephaly in Quebec: baseline prevalence, risk factors and outcomes in a large cohort of neonates.Carnitine palmitoyltransferase I and sudden unexpected infant death in British Columbia First Nations.The Genetics of Cardiovascular Disease in Canadian and International Aboriginal Populations.Spatial variability of gastroschisis in Canada, 2006-2011: An exploratory analysis.Human exposure to environmental contaminants and congenital anomalies: a critical review.Pre-eclampsia and risk of infantile haemangioma.Patient Recall, Interpretation, and Perspective of an Inconclusive Long QT Syndrome Genetic Test Result.Elevated ambient temperatures and risk of neural tube defects.Association Between Preeclampsia and Congenital Heart Defects.Maternal risk factors for gastroschisis in Canada.Spina bifida, folate metabolism, and dietary folate intake in a Northern Canadian aboriginal population.The development of a comprehensive maternal-child health information system for Nunavut-Nutaqqavut (Our Children).Hereditary angioedema managed with low-dose danazol and C1 esterase inhibitor concentrate: a case report.Pregnancy outcomes of women with spina bifida.
P50
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P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Laura Arbour
@ast
Laura Arbour
@en
Laura Arbour
@es
Laura Arbour
@nl
type
label
Laura Arbour
@ast
Laura Arbour
@en
Laura Arbour
@es
Laura Arbour
@nl
prefLabel
Laura Arbour
@ast
Laura Arbour
@en
Laura Arbour
@es
Laura Arbour
@nl
P106
P21
P31
P496
0000-0002-9589-0880