The genotypic and phenotypic spectrum of PIGA deficiency
Tarailo-Graovac, Maja, Sinclair, Graham, Stockler-Ipsiroglu, Sylvia, Van Allen, Margot, Rozmus, Jacob, Shyr, Casper, Biancheri, Roberta, Oh, Tracey, Sayson, Bryan, Lafek, Mirafe, Ross, Colin J, Robinson, Wendy P, Wasserman, Wyeth W, Rossi, Andrea, van Karnebeek, Clara D M
Published in Orphanet journal of rare diseases (27.02.2015)
Published in Orphanet journal of rare diseases (27.02.2015)
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Journal Article
Fetal Outcomes of Prenatally Diagnosed Congenital Diaphragmatic Hernia: Nine Years of Clinical Experience in a Canadian Tertiary Hospital
Oh, Tracey, MS, Chan, Stephanie, MSc, Kieffer, Stephanie, MS, Delisle, Marie-France, MD
Published in Journal of obstetrics and gynaecology Canada (2016)
Published in Journal of obstetrics and gynaecology Canada (2016)
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Journal Article
The Canadian genetic counseling workforce: Perspectives from employers and recent graduates
Costa, Taylor, Gillies, Brittany, Oh, Tracey, Scott, Jenna
Published in Journal of genetic counseling (01.04.2021)
Published in Journal of genetic counseling (01.04.2021)
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Journal Article
Mutations in ILK, encoding integrin-linked kinase, are associated with arrhythmogenic cardiomyopathy
Brodehl, Andreas, Rezazadeh, Saman, Williams, Tatjana, Munsie, Nicole M., Liedtke, Daniel, Oh, Tracey, Ferrier, Raechel, Shen, Yaoqing, Jones, Steven J.M., Stiegler, Amy L., Boggon, Titus J., Duff, Henry J., Friedman, Jan M., Gibson, William T., Childs, Sarah J., Gerull, Brenda
Published in Translational research : the journal of laboratory and clinical medicine (01.06.2019)
Published in Translational research : the journal of laboratory and clinical medicine (01.06.2019)
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Journal Article
Incidental finding of paternal UPD15 in a child with a deletion of 11q21-q22.3, presenting with developmental delay, coloboma and characteristic dysmorphic features
Tucker, Tracy, Steinraths, Michelle, Oh, Tracey, Nelson, Tanya N, Van Allen, Margot I, Brown, Lindsay, Schlade-Bartusiak, Kamilla
Published in Clinical dysmorphology (01.04.2016)
Published in Clinical dysmorphology (01.04.2016)
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Journal Article
Characterization of a new X‐linked mental retardation syndrome with microcephaly, cortical malformation, and thin habitus
du Souich, Christèle, Chou, Athena, Yin, Jingyi, Oh, Tracey, Nelson, Tanya N., Hurlburt, Jane, Arbour, Laura, Friedlander, Robin, McGillivray, Barbara C., Tyshchenko, Nataliya, Rump, Andreas, Poskitt, Kenneth J., Demos, Michelle K., Van Allen, Margot I., Boerkoel, Cornelius F.
Published in American journal of medical genetics. Part A (01.11.2009)
Published in American journal of medical genetics. Part A (01.11.2009)
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Journal Article
Outcome of prenatally diagnosed trisomy 6 mosaicism
Wallerstein, Robert, Oh, Tracey, Durcan, Judy, Abdelhak, Yaakov, Clachko, Mark, Aviv, Hana
Published in Prenatal diagnosis (01.08.2002)
Published in Prenatal diagnosis (01.08.2002)
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Journal Article
Characterization of a new X-linked mental retardation syndrome with microcephaly, cortical malformation, and thin habitus
du Souich, Christèle, Chou, Athena, Yin, Jingyi, Oh, Tracey, Nelson, Tanya N., Hurlburt, Jane, Arbour, Laura, Friedlander, Robin, McGillivray, Barbara C., Tyshchenko, Nataliya, Rump, Andreas, Poskitt, Kenneth J., Demos, Michelle K., Van Allen, Margot I., Boerkoel, Cornelius F.
Published in American Journal of Medical Genetics Part A (01.11.2009)
Published in American Journal of Medical Genetics Part A (01.11.2009)
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