Mary Ann Thomas

Mary Ann Thomas

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Mary Ann Thomas

Mary Ann Thomas

Publications by authors named "Mary Ann Thomas"

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Effects of Brief Depression and Anxiety Management Training on a US Army Division's Primary Care Providers.

Mil Med 2020 Jan 28. Epub 2020 Jan 28.

Uniformed Services University of Health Sciences, F. Edward Hébert School of Medicine, 4301 Jones Bridge Rd, Bethesda, MD 20814, USA.

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http://dx.doi.org/10.1093/milmed/usz443DOI Listing
January 2020

Next-Generation Sequencing Using a Cardiac Gene Panel in Prenatally Diagnosed Cardiac Anomalies.

J Obstet Gynaecol Can 2018 11;40(11):1417-1423

Department of Medical Genetics, Cumming School of Medicine, University of Calgary, Calgary, AB; Alberta Children's Hospital Research Institute, Calgary, AB. Electronic address:

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http://dx.doi.org/10.1016/j.jogc.2018.02.002DOI Listing
November 2018

Mosaic trisomy 1q: a recurring chromosome anomaly that is a diagnostic challenge and is associated with a Fryns-like phenotype.

Prenat Diagn 2017 Jun 23;37(6):602-610. Epub 2017 May 23.

Department of Medical Genetics, Alberta Children's Hospital, University of Calgary, Calgary, Canada.

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http://dx.doi.org/10.1002/pd.5058DOI Listing
June 2017

Review of the recurrent 8q13.2q13.3 branchio-oto-renal related microdeletion, and report of an additional case with associated distal arthrogryposis.

Am J Med Genet A 2016 11 19;170(11):2984-2987. Epub 2016 Aug 19.

Department of Medical Genetics, University of Calgary, Alberta, Canada.

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http://dx.doi.org/10.1002/ajmg.a.37695DOI Listing
November 2016

Prenatal Array Comparative Genomic Hybridization in Fetuses With Structural Cardiac Anomalies.

J Obstet Gynaecol Can 2016 07 6;38(7):619-26. Epub 2016 May 6.

Department of Medical Genetics, University of Calgary, Calgary AB; Department of Pediatrics, University of Calgary, Calgary AB; Alberta Children's Hospital Research Institute for Child and Maternal Health, University of Calgary, Calgary AB.

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http://dx.doi.org/10.1016/j.jogc.2016.02.010DOI Listing
July 2016

9p13.1p13.3 interstitial deletion: A case report and further delineation of a rare condition.

Am J Med Genet A 2016 Apr 5;170A(4):1095-8. Epub 2016 Jan 5.

Department of Medical Genetics, Cumming School of Medicine, Alberta Children's Hospital, University of Calgary, Calgary, Alberta, Canada.

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http://doi.wiley.com/10.1002/ajmg.a.37534
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http://dx.doi.org/10.1002/ajmg.a.37534DOI Listing
April 2016

Bilateral congenital lumbar hernias in a patient with central core disease--A case report.

Neuromuscul Disord 2016 Jan 5;26(1):56-9. Epub 2015 Nov 5.

Department of Medical Genetics, Alberta Children's Hospital, Calgary, Alberta, Canada; Department of Pediatrics, University of Calgary, Calgary, Alberta, Canada.

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http://dx.doi.org/10.1016/j.nmd.2015.10.011DOI Listing
January 2016

Copy number loss upstream of RAI1 uncovers gene expression regulatory region that may impact Potocki-Lupski syndrome diagnosis.

Mol Cytogenet 2015 5;8:75. Epub 2015 Oct 5.

Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, NAB2015, Houston, TX 77030 USA.

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http://dx.doi.org/10.1186/s13039-015-0179-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4594966PMC
October 2015

Asymptomatic tonsillar herniation in a neonate with cleidocranial dysplasia.

Pediatrics 2014 Feb 20;133(2):e455-7. Epub 2014 Jan 20.

Division of Neurology, Department of Pediatrics, and.

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http://dx.doi.org/10.1542/peds.2013-0478DOI Listing
February 2014

Monozygotic twins with variable expression of Van der Woude syndrome.

Am J Med Genet A 2011 Aug 7;155A(8):2008-10. Epub 2011 Jul 7.

Faculty of Medicine, University of Calgary, Calgary, Canada.

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http://dx.doi.org/10.1002/ajmg.a.34022DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3140610PMC
August 2011

Distinguishing iron-reducing from sulfate-reducing conditions.

Ground Water 2009 Mar-Apr;47(2):300-5. Epub 2009 Jan 22.

U.S. Geological Survey, South Carolina Water Science Center, Columbia, SC 29210, USA.

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http://dx.doi.org/10.1111/j.1745-6584.2008.00536.xDOI Listing
June 2009

Prenatal diagnosis of monosomy 1p36: a focus on brain abnormalities and a review of the literature.

Am J Med Genet A 2008 Dec;146A(23):3062-9

Department of Human Genetics, McGill University, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1002/ajmg.a.32563DOI Listing
December 2008

A LMNA splicing mutation in two sisters with severe Dunnigan-type familial partial lipodystrophy type 2.

J Clin Endocrinol Metab 2006 Jul 24;91(7):2689-95. Epub 2006 Apr 24.

Blackburn Cardiovascular Genetics Laboratory, Robarts Research Institute, London, Ontario, Canada.

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http://dx.doi.org/10.1210/jc.2005-2746DOI Listing
July 2006

Connexin mutation testing of children with nonsyndromic, autosomal recessive sensorineural hearing loss.

J Otolaryngol 2004 Jun;33(3):189-92

The F. Clarke Fraser Clinical Genetics Unit, Montreal, QC.

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http://dx.doi.org/10.2310/7070.2004.00189DOI Listing
June 2004

Lissencephaly with der(17)t(17;20)(p13.3;p12.2)mat.

Am J Med Genet A 2004 Jan;124A(3):292-5

F. Clarke Fraser Clinical Genetics Unit, Division of Medical Genetics, Department of Pediatrics, Montreal Children's Hospital, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1002/ajmg.a.20373DOI Listing
January 2004