Judith E Allanson

Judith E Allanson

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Judith E Allanson

Judith E Allanson

Publications by authors named "Judith E Allanson"

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The Gene Messenger Impact Project: An Innovative Genetics Continuing Education Strategy for Primary Care Providers.

J Contin Educ Health Prof 2016 ;36(3):178-85

Dr. Carroll: Professor, Sydney G. Frankfort Chair in Family Medicine, Department of Family and Community Medicine, Sinai Health System, University of Toronto, Toronto, Ontario, Canada. Dr. Grad: Associate Professor, McGill University, Herzl Family Practice Centre, Centre Médecine Familiale Herzl, Montréal, Quebec, Canada. Dr. Allanson: Department of Genetics, Children's Hospital of Eastern Ontario, Professor, Department of Paediatrics, University of Ottawa, Ottawa, Canada. Dr. Pluye: Full Professor, FRQS Senior Research Scholar, Department of Family Medicine, McGill University, Montréal, Quebec, Canada. Ms. Permaul: Research Associate, Ray D. Wolfe Department of Family Medicine, Sinai Health System, Toronto, Toronto, Ontario, Canada. Dr. Pimlott: Assistant Professor, University of Toronto, Family Practice Health Centre, Women's College Hospital, Toronto, Ontario, Canada. Dr. Wilson: Professor, School of Epidemiology, Public Health and Preventive Medicine, University of Ottawa, Ottawa, Canada.

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http://dx.doi.org/10.1097/CEH.0000000000000079DOI Listing
February 2018

Objective studies of the face of Noonan, Cardio-facio-cutaneous, and Costello syndromes: A comparison of three disorders of the Ras/MAPK signaling pathway.

Am J Med Genet A 2016 10 7;170(10):2570-7. Epub 2016 May 7.

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

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http://dx.doi.org/10.1002/ajmg.a.37736DOI Listing
October 2016

Elements of morphology: general terms for congenital anomalies.

Am J Med Genet A 2013 Nov 3;161A(11):2726-33. Epub 2013 Oct 3.

Departments of Pediatrics and Clinical Genetics, Academic Medical Center, University of Amsterdam, Amsterdam, Netherlands.

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http://doi.wiley.com/10.1002/ajmg.a.36249
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http://dx.doi.org/10.1002/ajmg.a.36249DOI Listing
November 2013

Elements of morphology: standard terminology for the external genitalia.

Am J Med Genet A 2013 Jun 6;161A(6):1238-63. Epub 2013 May 6.

Department of Pediatrics and Clinical Genetics, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

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http://dx.doi.org/10.1002/ajmg.a.35934DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4440541PMC
June 2013

Noonan syndrome.

Lancet 2013 Jan 10;381(9863):333-42. Epub 2013 Jan 10.

Department of Cardiology and Division of Genetics, Children's Hospital Boston, Boston, MA 02115, USA.

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https://linkinghub.elsevier.com/retrieve/pii/S01406736126102
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http://dx.doi.org/10.1016/S0140-6736(12)61023-XDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4267483PMC
January 2013

Special Section. Syndrome-specific growth charts.

Am J Med Genet A 2012 Nov 4;158A(11):2645-6. Epub 2012 Oct 4.

Department of Medical Genetics and Pediatrics, University of British Columbia and BC Children's Hospital Vancouver, British Columbia, Canada.

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http://doi.wiley.com/10.1002/ajmg.a.35704
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http://dx.doi.org/10.1002/ajmg.a.35704DOI Listing
November 2012

Brachial artery occlusion in a young adult with an ACTA2 thoracic aortic aneurysm.

Vasc Med 2012 Oct 3;17(5):326-9. Epub 2012 Sep 3.

Division of Cardiology, University of Ottawa Heart Institute, Ottawa, Ontario, Canada.

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http://dx.doi.org/10.1177/1358863X12453973DOI Listing
October 2012

Novel clinical findings in a case of postnatally diagnosed trisomy 12 mosaicism.

Am J Med Genet A 2012 Jun 14;158A(6):1452-4. Epub 2012 May 14.

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

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http://doi.wiley.com/10.1002/ajmg.a.35354
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http://dx.doi.org/10.1002/ajmg.a.35354DOI Listing
June 2012

Standard terminology for phenotypic variations: the elements of morphology project, its current progress, and future directions.

Hum Mutat 2012 May 13;33(5):781-6. Epub 2012 Apr 13.

1Division of Medical Genetics, Department of Pediatrics, University of Utah, Salt Lake City, Utah, USA.

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http://doi.wiley.com/10.1002/humu.22053
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http://dx.doi.org/10.1002/humu.22053DOI Listing
May 2012

Smith-Lemli-Opitz syndrome: Objective assessment of facial phenotype.

Am J Med Genet A 2012 May 21;158A(5):1020-8. Epub 2012 Mar 21.

Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada.

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http://dx.doi.org/10.1002/ajmg.a.35285DOI Listing
May 2012

Rett syndrome: a study of the face.

Am J Med Genet A 2011 Jul 27;155A(7):1563-7. Epub 2011 May 27.

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

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http://doi.wiley.com/10.1002/ajmg.a.34027
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http://dx.doi.org/10.1002/ajmg.a.34027DOI Listing
July 2011

Noonan syndrome: clinical features, diagnosis, and management guidelines.

Pediatrics 2010 Oct 27;126(4):746-59. Epub 2010 Sep 27.

Department of Pediatrics, Munger Pavilion, Room 123, New York Medical College, Valhalla, NY 10595, USA.

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http://dx.doi.org/10.1542/peds.2009-3207DOI Listing
October 2010

Trisomy 9p and Prader-Willi syndromes in an infant resulting from a de-novo unbalanced t(9;15) translocation.

Clin Dysmorphol 2009 Apr;18(2):103-6

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

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http://dx.doi.org/10.1097/MCD.0b013e328325ee66DOI Listing
April 2009

Elements of morphology: standard terminology for the head and face.

Am J Med Genet A 2009 Jan;149A(1):6-28

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

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http://dx.doi.org/10.1002/ajmg.a.32612DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778021PMC
January 2009

Elements of morphology: introduction.

Am J Med Genet A 2009 Jan;149A(1):2-5

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

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http://dx.doi.org/10.1002/ajmg.a.32601DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2774524PMC
January 2009

Noonan syndrome.

Am J Med Genet C Semin Med Genet 2007 Aug;145C(3):274-9

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

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http://dx.doi.org/10.1002/ajmg.c.30138DOI Listing
August 2007

Unrelated patients with a rearrangement of chromosome 2 causing duplication of 2p23 and deletion of 2q37.

Am J Med Genet A 2005 Apr;134(3):299-304

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

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http://dx.doi.org/10.1002/ajmg.a.30502DOI Listing
April 2005

3D analysis of facial morphology.

Am J Med Genet A 2004 May;126A(4):339-48

Eastman Dental Institute, UCL, London, United Kingdom.

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http://dx.doi.org/10.1002/ajmg.a.20665DOI Listing
May 2004

Holt-Oram syndrome: is there a "face"?

Am J Med Genet A 2003 May;118A(4):314-8

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

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http://dx.doi.org/10.1002/ajmg.a.10214DOI Listing
May 2003

De novo dup(X)(q22.3q26) in a girl with evidence that functional disomy of X material is the cause of her abnormal phenotype.

Am J Med Genet A 2003 Jan;116A(1):71-6

Eastern Ontario RegionalGenetics Program, Children's Hospital of Eastern Ontario, Ottawa, Canada.

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http://doi.wiley.com/10.1002/ajmg.a.10727
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http://dx.doi.org/10.1002/ajmg.a.10727DOI Listing
January 2003

A second family with blepharo-naso-facial syndrome.

Clin Dysmorphol 2002 Jul;11(3):191-4

Eastern Ontario Regional Genetics Program, Children's Hospital of Eastern Ontario, 401 Smyth Road, Ottawa, ON K1H 8L1, Canada.

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July 2002

Pitfalls of genetic diagnosis in the adolescent: the changing face.

Adolesc Med 2002 Jun;13(2):257-68, vi

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

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June 2002