Christine M Armour

Christine M Armour

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Christine M Armour

Christine M Armour

Publications by authors named "Christine M Armour"

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31Publications

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The value of diagnostic testing for parents of children with rare genetic diseases.

Genet Med 2019 12 26;21(12):2798-2806. Epub 2019 Jun 26.

Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON, Canada.

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http://dx.doi.org/10.1038/s41436-019-0583-1DOI Listing
December 2019

Genome-wide DNA methylation and RNA analyses enable reclassification of two variants of uncertain significance in a patient with clinical Kabuki syndrome.

Hum Mutat 2019 10 3;40(10):1684-1689. Epub 2019 Jul 3.

Department of Pathology and Laboratory Medicine, Western University, London, Ontario, Canada.

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http://dx.doi.org/10.1002/humu.23833DOI Listing
October 2019

NID1 variant associated with occipital cephaloceles in a family expressing a spectrum of phenotypes.

Am J Med Genet A 2019 05 17;179(5):837-841. Epub 2019 Feb 17.

Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.

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http://doi.wiley.com/10.1002/ajmg.a.61095
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http://dx.doi.org/10.1002/ajmg.a.61095DOI Listing
May 2019

Primary care providers' lived experiences of genetics in practice.

J Community Genet 2019 Jan 26;10(1):85-93. Epub 2018 Apr 26.

Department of Pediatrics, McMaster Children's Hospital, 1280 Main St. West, 3N11-G, Hamilton, ON, L8S 4K1, Canada.

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http://dx.doi.org/10.1007/s12687-018-0364-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325046PMC
January 2019

Trends in the use of prenatal testing services for fetal aneuploidy in Ontario: a descriptive study.

CMAJ Open 2018 Oct-Dec;6(4):E436-E444. Epub 2018 Oct 5.

Ontario Prenatal Screening Program, Better Outcomes Registry & Network (BORN) Ontario (Huang, Dougan, Walker, Armour, Okun), Ottawa, Ont.; Genetic Program (Huang), North York General Hospital, Toronto, Ont.; Regional Genetics Program (Armour), Children's Hospital of Eastern Ontario, Ottawa, Ont.; Maternal Fetal Medicine Program (Okun), Mt. Sinai Hospital, University of Toronto, Toronto, Ont.

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http://dx.doi.org/10.9778/cmajo.20180046DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182116PMC
October 2018

Broad spectrum of neuropsychiatric phenotypes associated with white matter disease in PTEN hamartoma tumor syndrome.

Am J Med Genet B Neuropsychiatr Genet 2018 Jan 20;177(1):101-109. Epub 2017 Nov 20.

Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.

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http://doi.wiley.com/10.1002/ajmg.b.32610
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http://dx.doi.org/10.1002/ajmg.b.32610DOI Listing
January 2018

Benchmarking outcomes in the Neonatal Intensive Care Unit: Cytogenetic and molecular diagnostic rates in a retrospective cohort.

Am J Med Genet A 2017 Jul 9;173(7):1839-1847. Epub 2017 May 9.

Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.

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http://dx.doi.org/10.1002/ajmg.a.38250DOI Listing
July 2017

Variable developmental delays and characteristic facial features-A novel 7p22.3p22.2 microdeletion syndrome?

Am J Med Genet A 2017 Jun 25;173(6):1593-1600. Epub 2017 Apr 25.

Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.

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http://dx.doi.org/10.1002/ajmg.a.38241DOI Listing
June 2017

Survey of the Definition of Fetal Viability and the Availability, Indications, and Decision Making Processes for Post-Viability Termination of Pregnancy for Fetal Abnormalities and Health Conditions in Canada.

J Genet Couns 2016 06 5;25(3):543-51. Epub 2015 Nov 5.

Regional Genetics Unit, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada.

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http://dx.doi.org/10.1007/s10897-015-9907-8DOI Listing
June 2016

Novel interstitial deletion of 10q24.3-25.1 associated with multiple congenital anomalies including lobar holoprosencephaly, cleft lip and palate, and hypoplastic kidneys.

Am J Med Genet A 2014 Dec 24;164A(12):3132-6. Epub 2014 Sep 24.

Department of Developmental Pediatrics, Montréal Children's Hospital, Montreal, Québec.

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http://dx.doi.org/10.1002/ajmg.a.36740DOI Listing
December 2014

Noninvasive prenatal testing from cell-free DNA.

CMAJ 2014 Sep 7;186(12):934. Epub 2014 Apr 7.

Eastern Ontario Regional Genetics Program, Department of Genetics (Armour, Nikkel), Children's Hospital of Eastern Ontario; Children's Hospital of Eastern Ontario Research Institute (Armour), Ottawa, Ont.

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http://dx.doi.org/10.1503/cmaj.131551DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4150709PMC
September 2014

A patient with an inborn error of vitamin B12 metabolism (cblF) detected by newborn screening.

Pediatrics 2013 Jul 17;132(1):e257-61. Epub 2013 Jun 17.

Department of Medical Genetics, Children’s Hospital of Eastern Ontario, Ottawa, Canada.

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http://dx.doi.org/10.1542/peds.2013-0105DOI Listing
July 2013

Microdeletion on 3p25 in a patient with features of 3p deletion syndrome.

Am J Med Genet A 2012 Oct 17;158A(10):2583-6. Epub 2012 Aug 17.

Department of Pediatrics, Queen's University, Kingston, Ontario, Canada.

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http://dx.doi.org/10.1002/ajmg.a.35559DOI Listing
October 2012

Fitzsimmons syndrome: spastic paraplegia, brachydactyly and cognitive impairment.

Am J Med Genet A 2009 Oct;149A(10):2254-7

Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.

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http://doi.wiley.com/10.1002/ajmg.a.33003
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http://dx.doi.org/10.1002/ajmg.a.33003DOI Listing
October 2009