Anna Lehman

Anna Lehman

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Anna Lehman

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Renpenning syndrome in a female.

Am J Med Genet A 2020 Mar 16;182(3):498-503. Epub 2019 Dec 16.

Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.

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http://dx.doi.org/10.1002/ajmg.a.61451DOI Listing
March 2020

De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature.

Eur J Hum Genet 2020 Jan 31. Epub 2020 Jan 31.

Centre de Génétique et Centre de Référence Maladies Rares (Anomalies du Développement de l'Interrégion Est), Hôpital d'Enfants, CHU Dijon Bourgogne, Dijon, France.

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http://dx.doi.org/10.1038/s41431-020-0571-6DOI Listing
January 2020

Strabismus in Children With Intellectual Disability: Part of a Broader Motor Control Phenotype?

Pediatr Neurol 2019 11 11;100:87-91. Epub 2019 Apr 11.

Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada; BC Children's Hospital and BC Women's Hospital, Vancouver, BC, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.pediatrneurol.2019.04.002DOI Listing
November 2019

Novel Exonic Deletions in TTC7A in a Newborn with Multiple Intestinal Atresia and Combined Immunodeficiency.

J Clin Immunol 2019 Aug 24;39(6):616-619. Epub 2019 Jul 24.

Department of Pathology and Laboratory Medicine, British Columbia Children's and Women's Hospital, The University of British Columbia, 4480 Oak St, Vancouver, BC, V6H3N1, Canada.

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http://dx.doi.org/10.1007/s10875-019-00669-6DOI Listing
August 2019

New developmental syndromes: Understanding the family experience.

J Genet Couns 2019 04 2;28(2):202-212. Epub 2019 Apr 2.

Department of Medical Genetics, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.

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http://doi.wiley.com/10.1002/jgc4.1121
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http://dx.doi.org/10.1002/jgc4.1121DOI Listing
April 2019

Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability.

Authors:
Benjamin Cogné Sophie Ehresmann Eliane Beauregard-Lacroix Justine Rousseau Thomas Besnard Thomas Garcia Slavé Petrovski Shiri Avni Kirsty McWalter Patrick R Blackburn Stephan J Sanders Kévin Uguen Jacqueline Harris Julie S Cohen Moira Blyth Anna Lehman Jonathan Berg Mindy H Li Usha Kini Shelagh Joss Charlotte von der Lippe Christopher T Gordon Jennifer B Humberson Laurie Robak Daryl A Scott Vernon R Sutton Cara M Skraban Jennifer J Johnston Annapurna Poduri Magnus Nordenskjöld Vandana Shashi Erica H Gerkes Ernie M H F Bongers Christian Gilissen Yuri A Zarate Malin Kvarnung Kevin P Lally Peggy A Kulch Brina Daniels Andres Hernandez-Garcia Nicholas Stong Julie McGaughran Kyle Retterer Kristian Tveten Jennifer Sullivan Madeleine R Geisheker Asbjorg Stray-Pedersen Jennifer M Tarpinian Eric W Klee Julie C Sapp Jacob Zyskind Øystein L Holla Emma Bedoukian Francesca Filippini Anne Guimier Arnaud Picard Øyvind L Busk Jaya Punetha Rolph Pfundt Anna Lindstrand Ann Nordgren Fayth Kalb Megha Desai Ashley Harmon Ebanks Shalini N Jhangiani Tammie Dewan Zeynep H Coban Akdemir Aida Telegrafi Elaine H Zackai Amber Begtrup Xiaofei Song Annick Toutain Ingrid M Wentzensen Sylvie Odent Dominique Bonneau Xénia Latypova Wallid Deb Sylvia Redon Frédéric Bilan Marine Legendre Caitlin Troyer Kerri Whitlock Oana Caluseriu Marine I Murphree Pavel N Pichurin Katherine Agre Ralitza Gavrilova Tuula Rinne Meredith Park Catherine Shain Erin L Heinzen Rui Xiao Jeanne Amiel Stanislas Lyonnet Bertrand Isidor Leslie G Biesecker Dan Lowenstein Jennifer E Posey Anne-Sophie Denommé-Pichon Claude Férec Xiang-Jiao Yang Jill A Rosenfeld Brigitte Gilbert-Dussardier Séverine Audebert-Bellanger Richard Redon Holly A F Stessman Christoffer Nellaker Yaping Yang James R Lupski David B Goldstein Evan E Eichler Francois Bolduc Stéphane Bézieau Sébastien Küry Philippe M Campeau

Am J Hum Genet 2019 03 28;104(3):530-541. Epub 2019 Feb 28.

Centre Hospitalier Universitaire Sainte-Justine Research Centre, University of Montreal, Montreal, QC H3T 1C5, Canada; Department of Pediatrics, University of Montreal, Montreal, QC H3T1J4, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2019.01.010DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407527PMC
March 2019

Genomic deletions upstream of lamin B1 lead to atypical autosomal dominant leukodystrophy.

Neurol Genet 2019 Feb 24;5(1):e305. Epub 2019 Jan 24.

Department of Human Genetics (B.N., Q.S.P.), Graduate School of Public Health, University of Pittsburgh; Department of Medical Sciences (E.G., A.B.), University of Torino, Italy; Department of Radiology (R.R.), Uppsala University, Sweden; Department of Medical Genetics (A.L.), British Columbia Children's Hospital, Vancouver, Canada; Department of Genome Sciences (M. Spielmann), University of Washington, Seattle; Department of Pediatrics (M.K.K., R.A., M.K.), McGovern Medical School, University of Texas, Houston; Departments of Clinical Genomics and Neurology (R.G.), Mayo Clinic, Rochester, MN; Department of Pathology (M.A.), King Abdulaziz University, Jeddah, Saudi Arabia; Department of Medical Imaging (M. Sharma), Western University, London, Canada; Departments of Pathology and Clinical Neurological Sciences (R.H.), Western University and London Health Sciences Centre, Canada; Office of the Clinical Director (W.A.G., C.T.), NHGRI; and NIH Undiagnosed Diseases Program (W.A.G., C.T.), Office of the Director, NIH, Bethesda, MD.

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http://dx.doi.org/10.1212/NXG.0000000000000305DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384018PMC
February 2019

Familial impairment of vocal cord mobility in childhood with clubfoot.

Clin Dysmorphol 2018 Oct;27(4):116-121

British Columbia Children's Hospital Research Institute.

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http://dx.doi.org/10.1097/MCD.0000000000000227DOI Listing
October 2018

The cost and diagnostic yield of exome sequencing for children with suspected genetic disorders: a benchmarking study.

Genet Med 2018 09 4;20(9):1013-1021. Epub 2018 Jan 4.

Collaboration for Outcomes Research and Evaluation (CORE), Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, British Columbia, Canada.

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http://dx.doi.org/10.1038/gim.2017.226DOI Listing
September 2018

Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders.

Am J Hum Genet 2018 01 21;102(1):175-187. Epub 2017 Dec 21.

Manchester Centre for Genomic Medicine, Division of Evolution & Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9WL, UK; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester M13 9WL, UK. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2017.11.013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5778085PMC
January 2018

p.Met233Val in a Complex Neurodegenerative Movement and Neuropsychiatric Disorder.

J Mov Disord 2018 Jan 11;11(1):45-48. Epub 2018 Jan 11.

Pacific Parkinson's Research Centre and Djavad Mowafaghian Centre for Brain Health, University of British Columbia, Vancouver, BC, Canada.

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http://dx.doi.org/10.14802/jmd.17066DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5790629PMC
January 2018

FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?

Am J Med Genet A 2017 Dec 8;173(12):3172-3181. Epub 2017 Sep 8.

Department of Pediatrics, University of South Dakota and Sanford Health, Sioux Falls, South Dakota.

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http://dx.doi.org/10.1002/ajmg.a.38462DOI Listing
December 2017

Correlation of novel PAX6 gene abnormalities in aniridia and clinical presentation.

Can J Ophthalmol 2017 Dec 6;52(6):570-577. Epub 2017 Jul 6.

Department of Ophthalmology and Visual Sciences, University of British Columbia, Vancouver, B.C. Electronic address:

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http://dx.doi.org/10.1016/j.jcjo.2017.04.006DOI Listing
December 2017

A novel RYR2 loss-of-function mutation (I4855M) is associated with left ventricular non-compaction and atypical catecholaminergic polymorphic ventricular tachycardia.

J Electrocardiol 2017 Mar - Apr;50(2):227-233. Epub 2016 Sep 8.

BC Inherited Arrhythmia Program, Vancouver, BC, Canada; Child and Family Research Institute, Vancouver, BC, Canada; Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.jelectrocard.2016.09.006DOI Listing
November 2017

High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.

Authors:
Fadi F Hamdan Candace T Myers Patrick Cossette Philippe Lemay Dan Spiegelman Alexandre Dionne Laporte Christina Nassif Ousmane Diallo Jean Monlong Maxime Cadieux-Dion Sylvia Dobrzeniecka Caroline Meloche Kyle Retterer Megan T Cho Jill A Rosenfeld Weimin Bi Christine Massicotte Marguerite Miguet Ledia Brunga Brigid M Regan Kelly Mo Cory Tam Amy Schneider Georgie Hollingsworth David R FitzPatrick Alan Donaldson Natalie Canham Edward Blair Bronwyn Kerr Andrew E Fry Rhys H Thomas Joss Shelagh Jane A Hurst Helen Brittain Moira Blyth Robert Roger Lebel Erica H Gerkes Laura Davis-Keppen Quinn Stein Wendy K Chung Sara J Dorison Paul J Benke Emily Fassi Nicole Corsten-Janssen Erik-Jan Kamsteeg Frederic T Mau-Them Ange-Line Bruel Alain Verloes Katrin Õunap Monica H Wojcik Dara V F Albert Sunita Venkateswaran Tyson Ware Dean Jones Yu-Chi Liu Shekeeb S Mohammad Peyman Bizargity Carlos A Bacino Vincenzo Leuzzi Simone Martinelli Bruno Dallapiccola Marco Tartaglia Lubov Blumkin Klaas J Wierenga Gabriela Purcarin James J O'Byrne Sylvia Stockler Anna Lehman Boris Keren Marie-Christine Nougues Cyril Mignot Stéphane Auvin Caroline Nava Susan M Hiatt Martina Bebin Yunru Shao Fernando Scaglia Seema R Lalani Richard E Frye Imad T Jarjour Stéphanie Jacques Renee-Myriam Boucher Emilie Riou Myriam Srour Lionel Carmant Anne Lortie Philippe Major Paola Diadori François Dubeau Guy D'Anjou Guillaume Bourque Samuel F Berkovic Lynette G Sadleir Philippe M Campeau Zoha Kibar Ronald G Lafrenière Simon L Girard Saadet Mercimek-Mahmutoglu Cyrus Boelman Guy A Rouleau Ingrid E Scheffer Heather C Mefford Danielle M Andrade Elsa Rossignol Berge A Minassian Jacques L Michaud

Am J Hum Genet 2017 Nov;101(5):664-685

Centre Hospitalier Universitaire Sainte-Justine Research Center, Montreal, QC H3T1C5, Canada; Department of Neurosciences, Université de Montréal, Montreal, QC H3T1J4, Canada; Department of Pediatrics, Université de Montréal, Montreal, QC H3T1C5, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2017.09.008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5673604PMC
November 2017

Genomic and Cytogenetic Characterization of a Balanced Translocation Disrupting NUP98.

Cytogenet Genome Res 2017 31;152(3):117-121. Epub 2017 Aug 31.

Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.

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http://dx.doi.org/10.1159/000479463DOI Listing
October 2017

Cost Analysis of Patients Referred for Inherited Heart Rhythm Disorder Evaluation.

Can J Cardiol 2017 06 20;33(6):814-821. Epub 2016 Dec 20.

Heart Rhythm Services, Division of Cardiology, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.cjca.2016.12.009DOI Listing
June 2017

Beyond the Electrocardiogram: Mutations in Cardiac Ion Channel Genes Underlie Nonarrhythmic Phenotypes.

Clin Med Insights Cardiol 2017 16;11:1179546817698134. Epub 2017 Mar 16.

British Columbia Inherited Arrhythmia Program and University of British Columbia, Vancouver, BC, Canada.

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http://dx.doi.org/10.1177/1179546817698134DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5392026PMC
March 2017

Patient Recall, Interpretation, and Perspective of an Inconclusive Long QT Syndrome Genetic Test Result.

J Genet Couns 2017 02 2;26(1):150-158. Epub 2016 Jul 2.

Department of Medical Genetics, University of British Columbia, Vancouver, Canada.

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http://link.springer.com/10.1007/s10897-016-9991-4
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http://dx.doi.org/10.1007/s10897-016-9991-4DOI Listing
February 2017

Hypogonadotropic Hypogonadism in Males with Glycogen Storage Disease Type 1.

JIMD Rep 2017 4;36:79-84. Epub 2017 Feb 4.

Division of Endocrinology, Vancouver General Hospital, University of British Columbia, Vancouver, BC, Canada.

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http://dx.doi.org/10.1007/8904_2016_38DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5680278PMC
February 2017

De Novo Mutations in EBF3 Cause a Neurodevelopmental Syndrome.

Am J Hum Genet 2017 Jan 23;100(1):138-150. Epub 2016 Dec 23.

Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford OX3 9DU, UK; Oxford Centre for Genomic Medicine, Nuffield Orthopaedic Centre, Oxford University Hospitals NHS Foundation Trust, Windmill Road, Headington, Oxford OX3 7HE, UK. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2016.11.020DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5223060PMC
January 2017

How do Physicians Decide to Refer Their Patients for Psychiatric Genetic Counseling? A Qualitative Study of Physicians' Practice.

J Genet Couns 2016 12 17;25(6):1235-1242. Epub 2016 May 17.

Department of Medical Genetics, University of British Columbia, Vancouver, Canada.

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http://dx.doi.org/10.1007/s10897-016-9961-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5173357PMC
December 2016

Etiologies of uterine malformations.

Am J Med Genet A 2016 08 8;170(8):2141-72. Epub 2016 Jun 8.

Department of Medical Genetics, University of British Columbia, Vancouver, Canada.

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http://doi.wiley.com/10.1002/ajmg.a.37775
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http://dx.doi.org/10.1002/ajmg.a.37775DOI Listing
August 2016

Exome Sequencing and the Management of Neurometabolic Disorders.

N Engl J Med 2016 Jun 25;374(23):2246-55. Epub 2016 May 25.

From the Centre for Molecular Medicine and Therapeutics (M.T.-G., C. Shyr, X.C.Y., L.-H.Z., J.J.Y.L., B.I.D., I.G., W.W.W., C.D.K.), the Departments of Medical Genetics (M.T.-G., C. Shyr, C.J.R., X.C.Y., J.J.Y.L., L.A., J.M.F., S.L., M.M., M.I.V.A., A.M.L., W.W.W.), Pediatrics (C.J.R., G.A.H., R.S., L.-H.Z., A.P.B., B.I.D., M.B.C., M.D., T.D., J.D., A. Michoulas, D.M., J.R., K.R.S., K.S., S.E.T., John Wu, S.S.-I., C.D.K.), and Pathology and Laboratory Medicine (B.R., P.E., H.V., G.S.), the Child and Family Research Institute (M.T.-G., C. Shyr, C.J.R., G.A.H., X.C.Y., A.P.B., J.J.Y.L., B.I.D., L.A., M.B.C., M.D., J.D., J.M.F., I.G., S.L., M.M., D.M., J.R., K.R.S., K.S., S.E.T., M.I.V.A., John Wu, P.E., A.M.L., H.V., S.S.-I., G.S., W.W.W., C.D.K.), and the Division of Endocrinology, Adult Metabolic Diseases Clinic (A. Mattman, S. Sirrs), University of British Columbia, and the Divisions of Biochemical Diseases (G.A.H., R.S., B.S., S.S.-I., C.D.K.), Pediatric Neurology (M.B.C., M.D., A. Michoulas, K.S.), Pediatric Nephrology (J.D.), Pediatric Endocrinology (D.M.), and Immunology (S.E.T.) and the Division of Hematology, Oncology and Transplantation, Michael Cuccione Childhood Cancer Research Program (J.R., K.R.S., John Wu), BC Children's Hospital, Vancouver, the Department of Pathology and Laboratory Medicine, Hospital for Sick Children, University of Toronto, Toronto (J.C.), the Department of Biological and Computing Sciences, University of Alberta (R.M., D.W.), and the National Institute for Nanotechnology (D.W.), Edmonton, AB, and the Department of Biomedical Physiology and Kinesiology, Simon Fraser University, Burnaby, BC (M. Abdelsayed, P.R.) - all in Canada; the Division of Genetics, Department of Pediatrics, King Saud Bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Riyadh, Saudi Arabia (M. Alfadhel); the Division of Metabolism and Children's Research Center, University Children's Hospital Zurich, Zurich (M.R.B., P.B.), and the Departmen

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http://dx.doi.org/10.1056/NEJMoa1515792DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4983272PMC
June 2016

BMPER variants associated with a novel, attenuated subtype of diaphanospondylodysostosis.

J Hum Genet 2015 Dec 15;60(12):743-7. Epub 2015 Oct 15.

Department of Medical Genetics, University of British Columbia, Vancouver, Canada.

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http://dx.doi.org/10.1038/jhg.2015.116DOI Listing
December 2015

A Clinical Classification Scheme for Tracheobronchomegaly (Mounier-Kuhn Syndrome).

Lung 2015 Oct 19;193(5):815-22. Epub 2015 Jul 19.

Department of Medical Genetics, University of British Columbia, C234-4500 Oak Street, Vancouver, BC, V6H 3N1, Canada.

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http://dx.doi.org/10.1007/s00408-015-9757-zDOI Listing
October 2015

Diffuse angiopathy in Adams-Oliver syndrome associated with truncating DOCK6 mutations.

Am J Med Genet A 2014 Oct 4;164A(10):2656-62. Epub 2014 Aug 4.

Department of Medical Genetics and Child and Family Research Institute, University of British Columbia, Vancouver, Canada.

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http://dx.doi.org/10.1002/ajmg.a.36685DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4167472PMC
October 2014

Mutations in NOTCH1 cause Adams-Oliver syndrome.

Am J Hum Genet 2014 Sep 14;95(3):275-84. Epub 2014 Aug 14.

Department of Medical Genetics and Child and Family Research Institute, University of British Columbia, Vancouver, BC V6H 3N1, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2014.07.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4157158PMC
September 2014

Anterolateral diaphragmatic hernia with body wall defect understood in relation to the abaxial domain.

Am J Med Genet A 2014 Jul 3;164A(7):1860-2. Epub 2014 Apr 3.

Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.

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http://doi.wiley.com/10.1002/ajmg.a.36529
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http://dx.doi.org/10.1002/ajmg.a.36529DOI Listing
July 2014

Mitochondrial carbonic anhydrase VA deficiency resulting from CA5A alterations presents with hyperammonemia in early childhood.

Am J Hum Genet 2014 Mar 13;94(3):453-61. Epub 2014 Feb 13.

Division of Biochemical Diseases, BC Children's Hospital, University of British Columbia, Vancouver, BC V6H 3V4, Canada; Department of Pediatrics, BC Children's Hospital, University of British Columbia, Vancouver, BC V6H 3V4, Canada; Treatable Intellectual Disability Endeavour in British Columbia, BC Children's Hospital, University of British Columbia, Vancouver, BC V5Z 4H4, Canada.

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http://dx.doi.org/10.1016/j.ajhg.2014.01.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3951944PMC
March 2014

Corneal findings in Parry-Romberg syndrome.

Can J Ophthalmol 2014 Feb;49(1):e2-5

University of British Columbia, Vancouver, B.C.

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http://dx.doi.org/10.1016/j.jcjo.2013.09.010DOI Listing
February 2014

Child Neurology: Krabbe disease: a potentially treatable white matter disorder.

Neurology 2012 Nov;79(19):e170-2

Division of Pediatric Neurology, Faculty of Medicine, University of British Columbia, Vancouver, Canada.

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http://dx.doi.org/10.1212/WNL.0b013e3182735c8bDOI Listing
November 2012

Emphysema in an adult with galactosialidosis linked to a defect in primary elastic fiber assembly.

Mol Genet Metab 2012 May 8;106(1):99-103. Epub 2012 Feb 8.

Department of Medical Genetics and the Child and Family Research Institute, University of British Columbia, Vancouver, Canada.

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http://dx.doi.org/10.1016/j.ymgme.2012.02.004DOI Listing
May 2012

A characteristic syndrome associated with microduplication of 8q12, inclusive of CHD7.

Eur J Med Genet 2009 Nov-Dec;52(6):436-9. Epub 2009 Sep 17.

Department of Medical Genetics, University of British Columbia, Canada.

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http://dx.doi.org/10.1016/j.ejmg.2009.09.006DOI Listing
February 2010

Childhood-onset hemiatrophy caused by unilateral morphea.

Clin Dysmorphol 2009 Oct;18(4):213-4

Department of Medical Genetics, University of British Columbia, Vancouver, Canada.

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https://insights.ovid.com/crossref?an=00019605-200910000-000
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http://dx.doi.org/10.1097/MCD.0b013e32832a9e0cDOI Listing
October 2009

Schinzel-Giedion syndrome: report of splenopancreatic fusion and proposed diagnostic criteria.

Am J Med Genet A 2008 May;146A(10):1299-306

Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.

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http://doi.wiley.com/10.1002/ajmg.a.32277
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http://dx.doi.org/10.1002/ajmg.a.32277DOI Listing
May 2008

Transcriptional regulation of BACE1, the beta-amyloid precursor protein beta-secretase, by Sp1.

Mol Cell Biol 2004 Jan;24(2):865-74

Department of Psychiatry, Brain Research Center, The University of British Columbia, Vancouver, British Columbia V6T 1Z3, Canada.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC343820PMC
http://dx.doi.org/10.1128/mcb.24.2.865-874.2004DOI Listing
January 2004

Long-term survivorship and quality of life after cytoreductive surgery plus intraperitoneal hyperthermic chemotherapy for peritoneal carcinomatosis.

Ann Surg Oncol 2003 Mar;10(2):155-62

Department of Internal Medicine, Section of Hematology and Oncology, The Surgical Oncology Service, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.

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http://dx.doi.org/10.1245/aso.2003.03.067DOI Listing
March 2003

Illness experience, depression, and anxiety in chronic fatigue syndrome.

J Psychosom Res 2002 Jun;52(6):461-5

Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada

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http://dx.doi.org/10.1016/s0022-3999(02)00318-5DOI Listing
June 2002